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Showing items 6421 to 6440 of 7642
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Applied by Mozambique for 7102.10.00: - Unsorted, 7102.21.00: -- Unworked or simply sawn, cleaved or bruted and 7102.31.00: -- Unworked or simply sawn, cleaved or bruted
The measure came into effect on 20 November 2016
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 20 November 2016
- Publication where the measure is specified
- Decreto n.º 25/2015, de 20 de Novembro
- Regulation where the measure is specified
- Regulation on Marketing of Diamonds, Precious Metals and Gems
- Country/Region applying the measure
- Mozambique
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- Raw diamond buyers, sellers, exporters and importers shall keep written and electronic databases for a period of 5 (five) years of daily records of purchases, sales, exports and imports, in which Buyers or sellers, the respective Mineral Deeds, the quantity and value of diamonds sold, bought, exported or imported.
- Reference of the measure
- Article 35(4)
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 7102.10.00 - Unsorted No 20 November 2016 7102.21.00 -- Unworked or simply sawn, cleaved or bruted No 20 November 2016 7102.31.00 -- Unworked or simply sawn, cleaved or bruted No 20 November 2016 - Description
- Diamonds
Precious metals
Gems
Countries/Regions affected by the measure.
- Description
- Kimberly Process member countries
-
Applied by Rwanda on the entire world for
The measure came into effect on 30 August 2012
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 30 August 2012
- Publication where the measure is specified
- Official Gazette nº 46 of 12/11/2012
- Regulation where the measure is specified
- Law No 32/2012 Of 30/08/2012 On The Implementation Of The Convention On The Prohibition Of The Development, Production, Stockpiling And Use Of Chemical Weapons And On Their Destruction
- Country/Region applying the measure
- Rwanda
- The rationale of the measure
- The purpose of this Law is to implement the Convention on the prohibition of the development, production, stockpiling and use of chemical weapons and on their destruction.
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- Any person who develops, produces, otherwise acquires, retains, transfers or uses toxic chemicals or their precursors to which any provision in Parts 6 and 9 of the verification Annex of the Convention on the prohibition of development, production, stockpiling, use of chemical weapons and their destruction applies must notify the National Authority of the following:
1° chemicals in his/her possession and their use;
2° establishment of a plant or its accessories and its location;
3° preparation and submission of annual reports on chemicals. - Reference of the measure
- Art 7
- Measure also domestic
- No
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out PG: 41 Chemical weapons Yes A. Toxic chemicals: (1) O-Alkyl (<C10, incl. cycloalkyl) alkyl (Me, Et, n-Pr or i-Pr)-phosphonofluoridates e.g. Sarin: O-Isopropyl methylphosphonofluoridate (107-44-8) Soman: O-Pinacolyl methylphosphonofluoridate (96-64-0) (2) O-Alkyl (<C10, incl. cycloalkyl) N,N-dialkyl (Me, Et, n-Pr or i-Pr) phosphoramidocyanidates e.g. Tabun: O-Ethyl N,N-dimethyl phosphoramidocyanidate (77-81-6) (3) O-Alkyl (H or <C10, incl. cycloalkyl) S-2-dialkyl (Me, Et, n-Pr or i-Pr)-aminoethyl alkyl (Me, Et, n-Pr or i-Pr) phosphonothiolates and corresponding alkylated or protonated salts e.g. VX: O-Ethyl S-2-diisopropylaminoethyl methyl phosphonothiolate (50782-69-9) (4) Sulfur mustards: 2-Chloroethylchloromethylsulfide (2625-76-5) Mustard gas: Bis(2-chloroethyl)sulfide (505-60-2) Bis(2-chloroethylthio)methane (63869-13-6) Sesquimustard: 1,2-Bis(2-chloroethylthio)ethane (3563-36-8) 1,3-Bis(2-chloroethylthio)-n-propane (63905-10-2) 1,4-Bis(2-chloroethylthio)-n-butane (142868-93-7) 1,5-Bis(2-chloroethylthio)-n-pentane (142868-94-8) Bis(2-chloroethylthiomethyl)ether (63918-90-1) O-Mustard: Bis(2-chloroethylthioethyl)ether (63918-89-8) Schedules of Chemicals 52 (5) Lewisites: Lewisite 1: 2-Chlorovinyldichloroarsine (541-25-3) Lewisite 2: Bis(2-chlorovinyl)chloroarsine (40334-69-8) Lewisite 3: Tris(2-chlorovinyl)arsine (40334-70-1) (6) Nitrogen mustards: HN1: Bis(2-chloroethyl)ethylamine (538-07-8) HN2: Bis(2-chloroethyl)methylamine (51-75-2) HN3: Tris(2-chloroethyl)amine (555-77-1) (7) Saxitoxin (35523-89-8) (8) Ricin (9009-86-3) B. Precursors: (9) Alkyl (Me, Et, n-Pr or i-Pr) phosphonyldifluorides e.g. DF: Methylphosphonyldifluoride (676-99-3) (10) O-Alkyl (H or <C10, incl. cycloalkyl) O-2-dialkyl (Me, Et, n-Pr or i-Pr)-aminoethyl alkyl (Me, Et, n-Pr or i-Pr) phosphonites and corresponding alkylated or protonated salts e.g. QL: O-Ethyl O-2-diisopropylaminoethyl methylphosphonite (57856-11-8) (11) Chlorosarin: O-Isopropyl methylphosphonochloridate (1445-76-7) (12) Chlorosoman: O-Pinacolyl methylphosphonochloridate (7040-57-5) unscheduled discrete organic chemicals unscheduled discrete organic chemical containing the elements phosphorus, sulfur or fluorine - Description
- A. Toxic chemicals:
(1) O-Alkyl (<C10, incl. cycloalkyl) alkyl
(Me, Et, n-Pr or i-Pr)-phosphonofluoridates
e.g. Sarin: O-Isopropyl methylphosphonofluoridate (107-44-8)
Soman: O-Pinacolyl methylphosphonofluoridate (96-64-0)
(2) O-Alkyl (<C10, incl. cycloalkyl) N,N-dialkyl
(Me, Et, n-Pr or i-Pr) phosphoramidocyanidates
e.g. Tabun: O-Ethyl N,N-dimethyl
phosphoramidocyanidate (77-81-6)
(3) O-Alkyl (H or <C10, incl. cycloalkyl) S-2-dialkyl
(Me, Et, n-Pr or i-Pr)-aminoethyl alkyl
(Me, Et, n-Pr or i-Pr) phosphonothiolates and
corresponding alkylated or protonated salts
e.g. VX: O-Ethyl S-2-diisopropylaminoethyl
methyl phosphonothiolate (50782-69-9)
(4) Sulfur mustards:
2-Chloroethylchloromethylsulfide (2625-76-5)
Mustard gas: Bis(2-chloroethyl)sulfide (505-60-2)
Bis(2-chloroethylthio)methane (63869-13-6)
Sesquimustard: 1,2-Bis(2-chloroethylthio)ethane (3563-36-8)
1,3-Bis(2-chloroethylthio)-n-propane (63905-10-2)
1,4-Bis(2-chloroethylthio)-n-butane (142868-93-7)
1,5-Bis(2-chloroethylthio)-n-pentane (142868-94-8)
Bis(2-chloroethylthiomethyl)ether (63918-90-1)
O-Mustard: Bis(2-chloroethylthioethyl)ether (63918-89-8)
Schedules of Chemicals 52
(5) Lewisites:
Lewisite 1: 2-Chlorovinyldichloroarsine (541-25-3)
Lewisite 2: Bis(2-chlorovinyl)chloroarsine (40334-69-8)
Lewisite 3: Tris(2-chlorovinyl)arsine (40334-70-1)
(6) Nitrogen mustards:
HN1: Bis(2-chloroethyl)ethylamine (538-07-8)
HN2: Bis(2-chloroethyl)methylamine (51-75-2)
HN3: Tris(2-chloroethyl)amine (555-77-1)
(7) Saxitoxin (35523-89-8)
(8) Ricin (9009-86-3)
B. Precursors:
(9) Alkyl (Me, Et, n-Pr or i-Pr) phosphonyldifluorides
e.g. DF: Methylphosphonyldifluoride (676-99-3)
(10) O-Alkyl (H or <C10, incl. cycloalkyl) O-2-dialkyl
(Me, Et, n-Pr or i-Pr)-aminoethyl alkyl
(Me, Et, n-Pr or i-Pr) phosphonites and
corresponding alkylated or protonated salts
e.g. QL: O-Ethyl O-2-diisopropylaminoethyl
methylphosphonite (57856-11-8)
(11) Chlorosarin: O-Isopropyl methylphosphonochloridate (1445-76-7)
(12) Chlorosoman: O-Pinacolyl methylphosphonochloridate (7040-57-5)
unscheduled discrete organic chemicals
unscheduled discrete organic chemical containing the elements phosphorus, sulfur or fluorine
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Rwanda on the entire world for
The measure came into effect on 15 August 2008
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 15 August 2008
- Publication where the measure is specified
- Ministerial Order Nº006/2008 Of 15/08/2008
- Regulation where the measure is specified
- Ministerial Order Nº006/2008 Of 15/08/2008 Regulating The Importation And Exportation Of Ozone Layer Depleting Substances Products And Equipment Containing Such Substances
- Country/Region applying the measure
- Rwanda
- The rationale of the measure
- The present Order shall regulate imports, exports and reexports of substances that deplete the Ozone Layer abbreviated as ODS, products and equipment containing such substances.
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- Application file for annual import quota by recognized importer should show management of ozone layer depleting products imported during the previous year
- Reference of the measure
- Art 9
- Measure also domestic
- No
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out PG: 36 Ozone-depleting substances Yes Annex 1 CFC-11 CFC-12 CFC-113 CFC-115 CFC-114 Halon-1211 Halon-1301 Halon-2402 Annex 2 CFC-13 CFC-111 CFC-112 CFC-211 CFC-212 CFC-213 CFC- 214 CFC-215 CFC-216 CFC-217 Carbon tetra chloride methyl chloroform or 1,1,1-trichloroethane Annex III HCFC-21 (3) HCFC-22 (3) HCFC-31 HCFC-121 HCFC-122 HCFC-123 (3) HCFC-124 (3) HCFC-131 HCFC-132 HCFC-133 HCFC-141 HCFC-141b (3) HCFC-142 HCFC-142b (3) HCFC-151 HCFC-221 HCFC-222 HCFC-223 HCFC-224 HCFC-225 HCFC-225ca (3) HCFC-225cb HCFC-226 HCFC-231 HCFC-232 HCFC-233 HCFC-234 HCFC-235 HCFC-241 HCFC-242 HCFC-243 HCFC-244 HCFC-251 HCFC-252 HCFC-253 HCFC-261 HCFC-262 HCFC-271 HBFC – 22B1 - Description
- Annex 1
CFC-11
CFC-12
CFC-113
CFC-115
CFC-114
Halon-1211
Halon-1301
Halon-2402
Annex 2
CFC-13
CFC-111
CFC-112
CFC-211
CFC-212
CFC-213
CFC- 214
CFC-215
CFC-216
CFC-217
Carbon tetra chloride
methyl chloroform or 1,1,1-trichloroethane
Annex III
HCFC-21 (3)
HCFC-22 (3)
HCFC-31
HCFC-121
HCFC-122
HCFC-123 (3)
HCFC-124 (3)
HCFC-131
HCFC-132
HCFC-133
HCFC-141
HCFC-141b (3)
HCFC-142
HCFC-142b (3)
HCFC-151
HCFC-221
HCFC-222
HCFC-223
HCFC-224
HCFC-225
HCFC-225ca (3)
HCFC-225cb
HCFC-226
HCFC-231
HCFC-232
HCFC-233
HCFC-234
HCFC-235
HCFC-241
HCFC-242
HCFC-243
HCFC-244
HCFC-251
HCFC-252
HCFC-253
HCFC-261
HCFC-262
HCFC-271
HBFC – 22B1
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Rwanda on the entire world for
The measure came into effect on 15 February 2012
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 15 February 2012
- Publication where the measure is specified
- Official Gazette n° 15 0f 09/04/2012
- Regulation where the measure is specified
- Law N°03/2012 Of 15/02/2012 Governing Narcotic Drugs, Psychotropic Substances And Precursors In Rwanda
- Country/Region applying the measure
- Rwanda
- The rationale of the measure
- This Law regulates the production, processing, distribution and use of narcotic drugs, psychotropic substances and precursors in Rwanda
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- Commercial documents such as invoices, manifest and customs or transport documents and other shipping documents shall indicate:
1º name in the common international denomination of narcotic drugs and psychotropic substances;
2º trade name;
3º quantity exported from the national territory or to be imported under that authorisation;
4º name and the address of the exporter;
5º importer;
6º indicate if the consignee is aware. - Reference of the measure
- Art 11
- Measure also domestic
- No
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out PG: 37 Narcotic drugs and psychotropic substances No - Description
- Narcotic drugs and psychotropic substances
Narcotic drugs
a. Table I: includes the chemicals that result into a heavy addiction and lead to abuse.
b. Table II: includes chemicals that cause less addiction and result into less abuse than that of table I.
c. Table III: includes the preparation containing narcotics made for medical legitimate purposes and composed in such a manner that they are less susceptible to be an object of abuse and cannot easily produce a narcotic drug.
d. Table IV: includes certain narcotic drugs named in table I that are considered as particularly harmful due to their properties and their use.
Psychotropic substances
a. Table I: includes prohibited chemicals that are of no medical interest.
b. Table II: includes chemicals that are of medical interest subjected to strictness.
c. Table III: includes the chemicals that are of medical interest, subjected to normal control.
d. Table IV: includes some of narcotic drugs named in table I that are considered as particularly
harmful due to their properties and their use.
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 25 October 2013
- Publication where the measure is specified
- Uganda Gazette Vol. CV No. 54 of 25th October 2013
- Regulation where the measure is specified
- US 1035:2013, Wood moisture meters — General provisions for verification methods and equipment
- Country/Region applying the measure
- Uganda
- Description of the measure
- This Uganda Standard prescribes the methods, equipment and conditions for the initial and periodic verifications of wood moisture meters. This standard covers all moisture meters, irrespective of their principles of operation.
- Reference of the measure
- US 1035:2013,
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- wood moisture meters
Countries/Regions affected by the measure.
-
Applied by South Africa on the entire world for 1001: Wheat and meslin. and 1005: Maize (corn).
The measure came into effect on 21 May 2004
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 21 May 2004
- Publication where the measure is specified
- STAATSKOERANT, 2 APRIL 2004 No. 26181 3 GOVERNMENT NOTICES GOEWERMENTSKENNISGEWINGS
- Regulation where the measure is specified
- MARKETING OF AGRICULTURAL PRODUCTS ACT, 1996 (ACT No. 47 OF 1996)
- Country/Region applying the measure
- South Africa
- The rationale of the measure
- The aim and objectives of this statutory measure are to compel any person directly and indirectly involved in imports and/or exports (e.g. end-consumers, importers, starers, exporters, processors, including any person, e.g. a producer, trader, transporter, agent,etc. who acts in the capacity of the aforementioned persons) of maize and/or wheat to keep records and submit returns to SAGIS. The statutory measure is deemed necessary in order to ensure that accurate import and export information in respect of maize and/or wheat is made available more frequently to all role-players and decision makers in the grain industry.
This statutory measure is deemed necessary to:
• Obtain complete and reliable information; and
• Assist the more efficient and effective planning, risk management and marketing of maize and/or wheat for food security.
SAGIS was specifically established for the purpose of handling information, gathering, processing and dissemination on behalf of the various cereal and oil seed industries in South Africa. This statutory measure will be administered by SAGIS but as a task separate to its main task of monthly national marketing information. SAGIS publishes macro maize and wheat import and export information on a regular basis for the grain industry and other interested parties. This information is obtained and furnished from the returns submitted to SAGIS. The information gathered by SAGIS by means of records and returns is available free of cost on SAGIS's website. This allows interested parties access whenever they need the information - Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- Records to be kept by end-consumers, importers, starers, exporters and processors of maize and/or wheat
5. (1) Each end-consumer, importer, storer, exporter and processor of maize and/or wheat shall keep complete records for each week (Saturday to Friday) in respect of maize and/or wheat imported or exported by him. These shall also include any person, e.g. a producer, trader, transporter, agent, etc. who acts in the capacity or on behalf of the aforementioned persons.
(2) Each person mentioned in sub clause (1), irrespective of whether or not he has premises, shall keep the following records:
(a) Imports- in respect of imported maize and/or wheat, records shall be kept of:
(i) Name and address of importer and/or person on whose behalf imports are made.
(ii) Quantity of maize and/or wheat imported per country of origin.
(iii) Quantity of imported maize and/or wheat destined for: (aa) consumption in South Africa.
(bb) exports per country of destination in Africa.
(cc) exports per country of destination overseas.
(iv) Name of border post through which maize and/or wheat was imported.
(v) Name and address of the first premises where maize and/or wheat, imported through a border post, was handled.
(vi) Name of harbor and owner of harbor premises where the imported maize and/or wheat was handled.
(vii) Name and particulars of the vessel in which maize and/or wheat was imported.
(b) Exports- in respect of maize and/or wheat that is exported, records shall be kept in respect of:
(i) Name and address of the exporter and/or the person on behalf of whom the export took place.
(ii) Quantity of maize and/or wheat exported per country of origin namely:
(aa) Produced in South Africa.
(bb) Imports per country of origin in Africa.
(cc) Imports per country of origin overseas.
(iii) Quantity of maize and/or wheat exported per land of intended destination.
(iv) Name and address of the last premises from where maize and/or wheat was dispatched to a border post.
(v) Name of border post through which maize and/or wheat was exported.
(vi) Name of harbor and owner of harbor premises where the exported maize and/or wheat was handled.
(vii) Name and particulars of the vessel in which maize and/or wheat was exported.
(3) Records mentioned in sub clauses (1) to (2) shall be -
(a) kept separately in respect of maize and/or wheat;
(b) recorded on a computer or in ink in a book; and
(c) kept at the head office or usual place of business of the person who is required to keep it for a period of at least four years after the end of the period in respect of which such records were kept.
Returns to be submitted by end-consumers, importers, starers, exporters and processors of maize and wheat
6.(1) Every end-consumer, importer, storer, exporter and processor of maize and/or wheat shall, before noon, on a Monday of every week, or in the case of public holidays on a Monday, the first working day of the week, submit to
SAGIS an accurate return in respect of his maize and/or wheat imports and/or exports. These shall also include any person, e.g. a producer, agent, trader, transporter etc. who acts in the capacity of the aforementioned persons.
(2) The returns, as available at SAGIS’ offices, shall be submitted for the physical exports and imports that realized during the period stated in clause 5(1).
(3) The return shall be transmitted electronically to:
The fax number or e-mail address as furnished on the official return forms or as specifically requested by SAGIS.
(4) The return shall be transmitted electronically to reach the general manager of SAGIS before or on the deadline date mentioned in sub clause (1).
(5) A zero return shall be submitted if no maize and/or wheat was handled, imported or exported during the period of the return. - Reference of the measure
- Section 5 & 6
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 1001 Wheat and meslin. Yes wheat 1005 Maize (corn). No - Description
- Maize and Wheat
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world 21 May 2004 - Description
- All countries
-
Applied by South Africa on the entire world for 0802.90: - Other and 2008.19: -- Other, including mixtures
The measure came into effect on 06 November 2015
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 06 November 2015
- Publication where the measure is specified
- GOVERNMENT Gazette 6/11/2015
- Regulation where the measure is specified
- MARKETING OF AGRICULTURAL PRODUCTS ACT, 1996 (ACT NO. 47 OF 1996)
- Country/Region applying the measure
- South Africa
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- Records to be kept and returns to be rendered
5. (1) All producers, processors, importers and exporters of pecan nuts and pecan nut products shall keep such records and render the returns as may be required by SAPPA relating to:
(a) Pecan nut trees;
(b) The volume of pecan nuts and/or pecan nut products produced; and
(c) The volume of pecan nuts and/or pecan nut products imported and/or exported.
(2) No records or returns shall be required in terms of this measure which disclose confidential information of a marketing nature, and in particular, no returns disclosing, inter alia, contracting parties; purchasers of pecan nuts products; prices of services or the prices obtained for product, or any similar information, shall be required to be furnished.
(3) The National Department of Agriculture, Forestry and Fisheries or its assignee shall render a copy of all export certificates or furnish the information required by SAPPA contained in such certificates within the period specified in sub- clause (4)
(4) The records referred to in sub-clause (1) shall –
(a) be recorded on a computer or with ink in a book;
(b) be kept at the registered premises of the person required to keep it for a period of at least three years.
(5) The returns referred to in sub-clause (1) shall be rendered on forms obtainable free of charge for this purpose from SAPPA within fifteen (15) days after the end of the month in which the returns have been requested - Reference of the measure
- No R 609
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 0802.90 - Other Yes pecan nuts 2008.19 -- Other, including mixtures Yes pecan nut products - Description
- pecan nuts and pecan nut products
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world 06 November 2015 - Description
- All countries
-
Applied by South Africa on the entire world for 1601: Sausages and similar products, of meat, meat offal or blood; food preparations based on these products. and 1602: Other prepared or preserved meat, meat offal or blood.
The measure came into effect on 09 September 2004
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 09 September 2004
- Publication where the measure is specified
- Government Notice R. 791 (Government Gazette 26531) of 9 July 2004
- Regulation where the measure is specified
- Compulsory Specification For The Manufacture, Production, Processing and Treatment of Canned Meat Products
- Country/Region applying the measure
- South Africa
- The rationale of the measure
- This specification specifies requirements for the manufacture, production, processing and treatment of canned meat products intended for human consumption.
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 12.2.1.11 Traceability and recall procedures
The record keeping system based on labelling records shall be established so that individual lots of the product in a consignment can be traced from the factory to the point of retail distribution. The recall procedures, when necessary, shall be established in consequence. - Reference of the measure
- Regulation 12.2.1.11
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 1601 Sausages and similar products, of meat, meat offal or blood; food preparations based on these products. Yes Canned meat products 1602 Other prepared or preserved meat, meat offal or blood. Yes Canned meat products - Description
- Canned meat products
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by South Africa on the entire world for 3923.21: -- Of polymers of ethylene and 3923.29: -- Of other plastics
The measure came into effect on 06 March 2014
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 06 March 2014
- Publication where the measure is specified
- Government Notice No. R. 651 (Government Gazette No. 36808) of 6 September 2013.
- Regulation where the measure is specified
- Compulsory Specification For Plastic Carrier Bags And Flat Bags - VC 8087
- Country/Region applying the measure
- South Africa
- The rationale of the measure
- 1.1 This compulsory specification covers the requirements for plastic carrier bags and flat bags that are made from virgin thermoplastics material or any percentage of recycled thermoplastics or filler materials that are intended for
use to carry products from a point of sale to use.
1.2 This compulsory specification does not apply to refuse bags, barrier bags, bin liners, household plastic bags, zip lock bags or carrier bags made from materials other than those specified in paragraph 1.1. - Description of the measure
- A.1 Application for Approval
The applicant shall apply to the NRCS for approval of every type of bag. The application shall be accompanied by the following:
A.1.1 Information on the construction (textured or non-textured) and material of the type of bag.
A1.2 Details of the manufacturing plant(s) where the type of bag is produced and/or the physical address where the imported products are received, stored or distributed from.
A1.3 Evidence of conformity, including test reports issued less than 12 months before the date of submission to the NRCS, by a conformity assessment body recognised in terms of the NRCS Conformity Assessment Policy, to prove
compliance with all the relevant requirements of this compulsory specification.
A1.4 The intended position of the approval number on the bag as set out in Section no. 4 of this compulsory specification.
A1.5 Information with regards to the body that will carry out the routine tests during the control of production.
A1.6 Any additional information relevant to the application for clarification purposes, as may be requested by the NRCS. - Reference of the measure
- Regulations A.1.1, A1.2, A1.4, A1.5 and A1.6
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 3923.21 -- Of polymers of ethylene Yes Plastic carrier bags and flat bags that are made from virgin thermoplastics material or any percentage of recycled thermoplastics or filler materials 3923.29 -- Of other plastics Yes Plastic carrier bags and flat bags that are made from virgin thermoplastics material or any percentage of recycled thermoplastics or filler materials - Description
- Plastic carrier bags and flat bags that are made from virgin thermoplastics material or any percentage of recycled thermoplastics or filler materials that are intended for use to carry products from a point of sale to use.
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by South Africa on the entire world for 8516.10: - Electric instantaneous or storage water heaters and immersion heaters and 8419.1: - Instantaneous or storage water heaters, non-electric :
The measure came into effect on 16 July 2014
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 16 July 2014
- Publication where the measure is specified
- Government Gazette No. 37631, 16 May 2014
- Regulation where the measure is specified
- The Compulsory Specification For Hot Water Storage Tanks For Domestic Use (VC9006)
- Country/Region applying the measure
- South Africa
- The rationale of the measure
- This compulsory specification covers the requirements for hot water storage tanks for domestic use. It includes fixed electrical storage water heaters; stand-alone water heaters and water containers, with or without heat exchangers or heating jackets, intended for use in solar heating and heat pump applications; and
tanks used for storage of hot water only. - Description of the measure
- A.1 Application for approval
The applicant shall apply to the NRCS for approval of every type of hot water storage tank. The application shall be accompanied by the following:
A.1.1 Technical specifications and drawings compiled in sufficient detail to identify the type and model of the hot water storage tank, method of assembly, and materials of construction.
A.1.2 Details of the manufacturing plant/s where the hot water storage tank is produced;
A.1.3 Evidence of conformity including test reports by a conformity assessment body recognized in terms of the NRCS's Conformity Assessment Policy issued less than 12 months before the date of submission to the NRCS, that prove compliance with all the requirements of this compulsory specification;
A.1.4 The markings to be applied to each type and model of hot water storage tank;
A.1.5 Information for users including instructions for use;
A.1.6 Information to the satisfaction of the NRCS regarding the measures taken by the applicant to ensure ongoing conformity with the mandatory requirements of this compulsory specification; and
A.1.7 Any reasonable additional information in order to clarify the above that may be requested by the NRCS. - Reference of the measure
- Regulations A.1.1, A.1.2, A.1.4, A.1.5, A.1.6 and A.1.7
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 8516.10 - Electric instantaneous or storage water heaters and immersion heaters No 8419.1 - Instantaneous or storage water heaters, non-electric : No - Description
- Hot water storage tanks for domestic use including fixed electrical storage water heaters; stand-alone water heaters and water containers, with or without heat exchangers or heating jackets, intended for use in solar heating and heat pump applications; and tanks used for storage of hot water only.
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by South Africa on the entire world for 2523: Portland cement, aluminous cement, slag cement, supersulphate cement and similar hydraulic cements, whether or not coloured or in the form of clinkers.
The measure came into effect on 06 September 2007
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 06 September 2007
- Publication where the measure is specified
- Government Notice No. R. 544 (Government Gazette 30023) of 6 July 2007
- Regulation where the measure is specified
- Compulsory Specification for Cement
- Country/Region applying the measure
- South Africa
- The rationale of the measure
- This compulsory specification covers the requirements for the manufacture, marking, properties and performance of cement, intended for construction use, irrespective of whether distributed in bulk or bagged form.
- Description of the measure
- 3.9 The importer shall notify the Regulator in advance of every consignment to be imported. The consignment may be made up of a number of smaller deliveries of the same cement product , as in the case of deliveries by road.
3.10 The manufacturer and/ or importer and certification body shall each undertake , in writing , to immediately report any failure to conform to the requirements of the compulsory specifications , of whatever nature, to the Regulator. - Reference of the measure
- Regulations 3.9 and 3.10
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 2523 Portland cement, aluminous cement, slag cement, supersulphate cement and similar hydraulic cements, whether or not coloured or in the form of clinkers. No - Description
- Cement i.e A hydraulic binder used for construction purposes described in either SANS 50197-1 Common cements, or SANS 50413-1 Masonry cement.
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 3004.90.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3004.90.20: Preparations containing a drug not categorised as prescription preparation and 3004.90.90: Other
The measure came into effect on 11 September 2015
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 11 September 2015
- Publication where the measure is specified
- Statutory Instrument 97 of 2015
- Regulation where the measure is specified
- Medicines and Allied Substances Control (Complementary Medicines) Regulations, 2015
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not stated in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 9. (1) For the purposes of subsection (6)(b) - 'finished product “in relation to a complementary medicine means complementary medicine which is wholly manufactured outside Zimbabwe and is imported into Zimbabwe and is ready for sale without having to be relabelled or repackaged.
(2) Any person who is required to make an application shall complete the appropriate form and shall furnish theDirector- General, or some other person appointed by him or her , with such further information or particulars as may be required.
(3) An application for the approval of a complementarymedicine may be made by –
(a) thePrincipal; or
(b) any other person acceptable to the Authority.
(4) Every application for the approval of a complementarymedicine shall be submitted in form C.M.1 in duplicate.
(5) In addition to subsection (4) , such application shall be accompanied by the following –
(a ) a sample of the complementarymedicine in the smallest of each of the package formavailable for distribution to the public including the identification marks on such complementary complimentary medicinewhere appropriate, or if such package forms are not yet available , a sample in package , in which the applicant intends to make the complementarymedicineavailable for distribution to the public; and (b) detailed information of all package inserts which the applicant intends to use; and
(c) such samples of the complementarymedicine or the raw materials thereof as the Authority may request for the analysis; and
(d) a single copy of any literature in support of the application. Provided that the Authority may require additional copies of such literature.
(e) a draft package insert or where there is no package insert, three labels or copies of the package and
(f) one copy of all records and batch data relating to a particular batch , where appropriate or possible, which shall include raw material analytical reports, master sheets relating to manufacture and packaging , in-process control records, final product analytical records and authorization for release , and any other relevant records; and
(g) theappropriate fee, together with such additional fee as may be fixed by the authority for thepurpose of analysing such complimentary medicines .
(6) Every applicantshall, without delay inform the authority either before or after the approval of a complementary medicine-
(a) of any alteration from the information or particularsfurnished by him or her in applying for approval in terms of subsections (4) and (5) ; and
(b) whether the complementary medicine is to be imported as a finished product , into or relabelled or repackaged or dealt with in any manner in Zimbabwe. - Reference of the measure
- Art 9(5)(f)
- Measure also domestic
- No
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 3004.90.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3004.90.20 Preparations containing a drug not categorised as prescription preparation No 3004.90.90 Other No - Description
- Aromatherapeutic substances, Ayurvedic Medicines, Energy Substances or Medicines, Homeopathic Remedies, Nutritional Substance in pharmaceutical form, Traditional Chinese Medicines, Traditional Dutch Remedies, Unanni Tibb Medicines, Western Herbal Medicines and such other medicines or remedies as may be approved by the Authority
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 3003.10.00: Containing penicillins or derivatives thereof, with a penicillinic acid structure, or streptomycin or their derivatives, 3003.31.00: Containing insulin, 3003.31.00: Containing insulin, 3003.39.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3003.39.90: Other, 3003.40.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3003.40.90: Other, 3003.90.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3003.90.90: Other, 3004.10.00: Containing penicillins or derivatives thereof, with a penicillanic acid structure, or streptomycins or their derivatives, 3004.20.00: Containing other antibiotics, 3004.31.00: Containing insulin, 3004.32.00: Containing corticosteroid hormones, their derivatives or structural analogues, 3004.39.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3004.39.90: Other, 3004.40.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3004.40.90: Other, 3004.50.00: Other medicaments containing vitamins or other products of heading 29.36, 3004.90.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3004.90.20: Preparations containing a drug not categorised as prescription preparation, 3004.90.90: Other, 3003.10.00: Containing penicillins or derivatives thereof, with a penicillinic acid structure, or streptomycin or their derivatives, 3003.31.00: Containing insulin, 3003.31.00: Containing insulin, 3003.39.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3003.39.90: Other, 3003.40.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3003.40.90: Other, 3003.90.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3003.90.90: Other, 3004.10.00: Containing penicillins or derivatives thereof, with a penicillanic acid structure, or streptomycins or their derivatives, 3004.20.00: Containing other antibiotics, 3004.31.00: Containing insulin, 3004.32.00: Containing corticosteroid hormones, their derivatives or structural analogues, 3004.39.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3004.39.90: Other, 3004.40.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3004.40.90: Other, 3004.50.00: Other medicaments containing vitamins or other products of heading 29.36, 3004.90.10: Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health, 3004.90.20: Preparations containing a drug not categorised as prescription preparation and 3004.90.90: Other
The measure came into effect on 01 July 2008
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 01 July 2008
- Publication where the measure is specified
- Statutory Instrument 57 of 2008
- Regulation where the measure is specified
- Medicines and Allied Substances Control (Import and Export of Medicines) Regulations, 2008.
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- These regulations shall apply to all medicines other than—
(a) those controlled in terms of the Dangerous Drugs Act [Chapter 15:02]; and
(b) psychotropic substances controlled in terms of the Medicines and Allied Substances
Control (General) Regulations, 1991; and
(c) medicines imported in terms of section 75 of the Act for a named person; and
(d) medicines imported by an individual for personal use. - Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 12. In addition to such terms and conditions as may be fixed in a permit to import or export any medicine, the importer or the exporter of any medicine shall comply with the following conditions—
(a) no import or export of any medicine shall be done through ordinary or registered post; and
(b) the importer or exporter of any medicine shall notify the Authority, within 30 days of the import or export of any medicine by him or her and the notification shall be made in Form I.E. 7. - Reference of the measure
- Art 12(b)
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 3003.10.00 Containing penicillins or derivatives thereof, with a penicillinic acid structure, or streptomycin or their derivatives No 3003.31.00 Containing insulin No 3003.31.00 Containing insulin No 3003.39.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3003.39.90 Other No 3003.40.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3003.40.90 Other No 3003.90.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3003.90.90 Other No 3004.10.00 Containing penicillins or derivatives thereof, with a penicillanic acid structure, or streptomycins or their derivatives No 3004.20.00 Containing other antibiotics No 3004.31.00 Containing insulin No 3004.32.00 Containing corticosteroid hormones, their derivatives or structural analogues No 3004.39.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3004.39.90 Other No 3004.40.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3004.40.90 Other No 3004.50.00 Other medicaments containing vitamins or other products of heading 29.36 No 3004.90.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3004.90.20 Preparations containing a drug not categorised as prescription preparation No 3004.90.90 Other No 3003.10.00 Containing penicillins or derivatives thereof, with a penicillinic acid structure, or streptomycin or their derivatives No 3003.31.00 Containing insulin No 3003.31.00 Containing insulin No 3003.39.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3003.39.90 Other No 3003.40.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3003.40.90 Other No 3003.90.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3003.90.90 Other No 3004.10.00 Containing penicillins or derivatives thereof, with a penicillanic acid structure, or streptomycins or their derivatives No 3004.20.00 Containing other antibiotics No 3004.31.00 Containing insulin No 3004.32.00 Containing corticosteroid hormones, their derivatives or structural analogues No 3004.39.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3004.39.90 Other No 3004.40.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3004.40.90 Other No 3004.50.00 Other medicaments containing vitamins or other products of heading 29.36 No 3004.90.10 Medicaments used in the management of chronic illnesses; approved by the secretary responsible for health No 3004.90.20 Preparations containing a drug not categorised as prescription preparation No 3004.90.90 Other No - Description
- These regulations apply to all medicines other than
(a)Psychotropic substances (Amphetamine, Dexamphetamine, Methamphetamine, Methylphenidate, Phencyclidine, Amobarbital, Cyclobarbital, Pentobarbital, Secobarbital, Amfepramone, Barbital, Ethinamate, Meprobamate, Methylphenobarbital, Phenobarbital, Pipradrol)
(b)Drugs controlled in terns of the Dangerous Drug Act ( coca leaves; “Indian hemp”, “bhang”, “camba”, “dagga”, “mbanje” or “intsangu”, resins obtained therefrom and all preparations of which such resins form the base; raw opium;1.Medicinal opium.
2. Any medicinal extract or tincture derived from the plant Cannabis sativa L. and any
preparation, not being a preparation capable of external use only, made from such
medicinal extract or tincture.
3. Morphine and its salts.
4. Cocaine (including synthetic cocaine) and ecgonine and their respective salts, and the
esters of ecgonine and their respective salts. (For the purposes of this Act, the expression
“ecgonine” means laevo-ecgonine and includes any derivatives of ecgonine from which it
may be recovered industrially.)
5. Any solution or dilution of morphine or cocaine or their salts in an inert substance,
whether liquid or solid, containing any proportion of morphine or cocaine, and any
preparation, admixture, extract or other substance (not being such a solution or dilution as
aforesaid) containing not less than one-fifth per centum of morphine or one-tenth per
centum of cocaine or of ecgonine.
6. Diacetylmorphine (commonly known as diamorphine or heroin) and the other esters of
morphine and their respective salts.
7. Dihydrohydroxycodeinone (also known as oxycodone);
Dihydrocodeinone (also known as hydrocodone);
Dihydromorphinone (also known as hydromorphone);
Acetyldihydrocodeinone;
Dihydromorphine;
their esters, and the salts of any of these substances and of their esters.
8. Morphine-N-oxide (commonly known as genomorphine) also the morphine-N-oxide
derivatives, and the other pentavalent nitrogen morphine derivatives. )
(c) Any medicines exempted from the operation of any or all of the provisions of the Medicines and Allied Substance Control Act
(d) The Regulations also excludes medicines imported by an individual for personal use.
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 3808.91.10: Insecticides in containers exceeding 20l or 5kg, 3808.91.90: Other, 3808.92.10: Fungicides in containers exceeding 20l or 5kg, 3808.92.90: Other, 3808.93.10: In containers exceeding 20 l or 5 kg, 3808.93.90: Other, 3808.94.10: In containers exceeding 20 l or 5 kg, 3808.94.90: Other, 3808.99.90: Other and 3808.99.90: Other
The measure came into effect on 21 September 2012
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 21 September 2012
- Publication where the measure is specified
- Statutory Instrument 144 of 2012
- Regulation where the measure is specified
- Pesticides Regulations, 2012
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not stated in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 8.(1) Any person who wishes to import into Zimbabwe any pesticides may apply for a permit to do so, if such a person's core business is the buying and the selling of pesticides:
Provided the pesticides are locally registered and bear the company name, registration number, pesticide name and formulation, source of pesticide, amount paid for pesticides and receipt number and expiry date for pesticides.
(2) An application for an import of pesticides permit shall be made in wiring to a registering officer in the Form P.5 prescribed in the First Schedule together with the payment of a prescribed fee:
Provided that imports of pesticides permit shall be valid –
(i) for sixty days from the date of issue if the source is within SADC region; and
(ii) (ii) for ninety days from the date of issue if the source is outside the SADC region and Africa; and
(iii) (iii) for one consignment only and in terms of the source specified in the registration certificate - Reference of the measure
- Art 8 (1)
- Measure also domestic
- No
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 3808.91.10 Insecticides in containers exceeding 20l or 5kg No 3808.91.90 Other No 3808.92.10 Fungicides in containers exceeding 20l or 5kg No 3808.92.90 Other No 3808.93.10 In containers exceeding 20 l or 5 kg No 3808.93.90 Other No 3808.94.10 In containers exceeding 20 l or 5 kg No 3808.94.90 Other No 3808.99.90 Other No 3808.99.90 Other No - Description
- Pesticides
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 2914.11.00: Acetone, 2915.24.00: Acetic anhydride, 2922.43.00: Anthranilic acid and its salts, 2939.41.00: Ephedrine and its salts, 2939.61.00: Ergometrine (inn) and its salts, 2806.10.00: Hydrogen chloride (hydrochloric acid), 2807.00.00: Sulphuric acid; oleu, 2932.94.00: Safrole, 2939.42.00: Pseudoephedrine (inn) and its salts and 2841.61.00: Potassium permanganate
The measure came into effect on 01 July 2008
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 01 July 2008
- Publication where the measure is specified
- Statutory Instrument 56 of 2008
- Regulation where the measure is specified
- Medicines and Allied Substances Control (Import and Export of Precursors and Certain Chemical Substances) Regulations, 2008
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not specified in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 5. Any person who imports or exports a substance listed in the Second Schedule shall, before the 31st March in each year, submit a return to the Authority stating the amounts so imported or exported from January to December in the preceding year.
- Reference of the measure
- Art 5
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 2914.11.00 Acetone No 2915.24.00 Acetic anhydride No 2922.43.00 Anthranilic acid and its salts No 2939.41.00 Ephedrine and its salts No 2939.61.00 Ergometrine (inn) and its salts No 2806.10.00 Hydrogen chloride (hydrochloric acid) No 2807.00.00 Sulphuric acid; oleu No 2932.94.00 Safrole No 2939.42.00 Pseudoephedrine (inn) and its salts No 2841.61.00 Potassium permanganate No - Description
- N-Acetylanthranilic acid (2);
Acetone;
Acetic anhydride;
Anthranilic acid;
Ephedrine; Ethyl ether;
Ergometrine;
Hydrochloric Acid (1) (2);
Ergotamine;
Methyl ethyl ketone (2);
Isosafrole (2);
Phenylacetic acid;
Lysergic acid;
Piperidine;
3,4 Methylenediooxyphenyl-2-propanone (2);
Sulphuric acid (1) (2);
Norephedrine; Toluene (2).
1-Phenyl-2-propanone;
Piperonal;
Potassium permanganate (2);
Pseudoephedrine;
Safrole (2).
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 1211.30.00: Coca leaf, 1211.90.00: Other and 1302.11.00: Opium
The measure came into effect on 01 January 1976
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 01 January 1976
- Publication where the measure is specified
- Rhodesia Government Notice No. 1111 of 1975
- Regulation where the measure is specified
- Dangerous Drugs Regulations,1975
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not specified in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 9. Every person authorized or licensed to supply Part II drugs shall–
(a) keep, in accordance with the provisions of this section and section 42, a register, and enter therein, in chronological sequence in the form specified in the Third Schedule, true particulars with respect to–
(i) every quantity of a Part II drug acquired by him;
(ii) every quantity of a Part II drug supplied by him;
(iii) every quantity of a Part II drug used by him;
(b) use a separate part of his register for entries relating to–
(i) raw opium
(ii) coca-leaves
(iii) indian hemp and the resins obtained from Indian hemp, and all preparations, other than extract and tincture of Indian hemp, of which such resins form the base. - Reference of the measure
- Art 9
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 1211.30.00 Coca leaf No 1211.90.00 Other Yes dagga 1302.11.00 Opium No - Description
- "(a) coca leaves;
(b) “Indian hemp”, “bhang”, “camba”, “dagga”, “mbanje” or “intsangu”, resins obtained therefrom and all preparations of which such resins form the base;
(c) raw opium."
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 1302.11.00: Opium, 2939.11.00: Concentrates of poppy straw; buprenorphine (inn), codeine, dihydrocodine(inn), ethylmorphine, etorphine (inn), heroin, hydrocodone (inn),hydromorphone (inn), morphine, nicomorphine (inn),oxycodone (inn), oxymorphone (inn), pholcodine (inn), thebacon (in, 2939.91.00: Cocaine, ecgonine, levometamfetamine, metamfetamine (inn), metamfetamine racemate ; salts, esters and other derivatives thereof, 2933.39.90: Other, 2922.31.00: Amfepramone (inn), methadone (inn) and normethadone (inn); salts thereof and 2939.19.00: Other
The measure came into effect on 01 January 1976
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 01 January 1976
- Publication where the measure is specified
- Rhodesia Government Notice No. 1111 of 1975
- Regulation where the measure is specified
- Dangerous Drugs Regulations,1975
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not specified in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 28. (1) Every person authorized or licensed to supply Part IV drugs or Part IV preparations shall–
(a) keep, in accordance with the provisions of this section and section 42, a register and shall enter therein, in chronological sequence, in the form specified in the Third Schedule, true particulars with respect to–
(i) every quantity of a Part IV drug or Part IV preparation acquired by him; and
(ii) every quantity of a Part IV drug or Part IV preparation supplied by him and
(iii) every quantity of a Part IV drug or Part IV preparation used by him;
(iv) every quantity of a Part IV drug or Part IV preparation manufactured by him.
[inserted by S.I. 409 of 1999]
(b) use a separate page in the register for each Part IV drug or Part IV preparation specified in the Fourth Schedule - Reference of the measure
- Art 28(1)(a) and (b)
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 1302.11.00 Opium Yes medicinal 2939.11.00 Concentrates of poppy straw; buprenorphine (inn), codeine, dihydrocodine(inn), ethylmorphine, etorphine (inn), heroin, hydrocodone (inn),hydromorphone (inn), morphine, nicomorphine (inn),oxycodone (inn), oxymorphone (inn), pholcodine (inn), thebacon (in No 2939.91.00 Cocaine, ecgonine, levometamfetamine, metamfetamine (inn), metamfetamine racemate ; salts, esters and other derivatives thereof No 2933.39.90 Other No 2922.31.00 Amfepramone (inn), methadone (inn) and normethadone (inn); salts thereof No 2939.19.00 Other No - Description
- 1. Medicinal opium.
2. Any extract or tincture of Indian hemp, and any preparation, not being a preparation capable of external use only, made from extract of tincture of Indian hemp.
3. Morphine and its salts, and any solution of dilution of morphine or its salts in an inert substance, whether liquid or solid, containing any proportion of morphine, and any preparation, admixture, extract or other substance (not being such a solution or dilution as aforesaid) containing not less than one-fifth of one percent of morphine (calculated in respect of anhydrous morphine).
4. Diacetylmorphine (also known as diamorphine or heroin) and its salts, and any solution or dilution of cocaine or its salts, and any preparation, admixture, extract or other substance containing any proportion of diacetylmorphine.
5. Cocaine (including synthetic cocaine) and ecgonine and their respective salts, and any solution or dilution of cocaine or its salts in an inert substance, whether liquid or solid, containing any proportion of cocaine, and any preparation, admixture, extract or other substance (not being such a solution or dilution as afore said) containing not less than one-tenth of one per cent of cocaine or any proportion of ecgonine.
6. Dihydrohydroxycodeinone (also known as eucodal) and its salts, and any preparation, admixture, extract or other substance containing any proportion of dihydrohydroxycodeinone or its salts.
7. Dihydrocodeinone (also known as dicodide) and its salts, and any preparation, admixture, extract or other substance containing any proportion of dihydrocodeinone or its salts.
8. Dihydromorphinone (also known as dilaudide) and its salts and any preparation, admixture, extract or other substance containing any proportion of dihydromorphinone or its salts.
9. 6-methyldihydromorphine and its salts, and any preparation, admixture, extract or other substance containing any proportion of 6-methyldihydromorphine or its salts.
10. Acetyldihyrocodeinone and its salts and any preparation, admixture, extract or other substance containing any proportion of acetyldihyrocodeinone or its salts.
11. Dihydromorphine and its salts, and any preparation, admixture, extract or other substance containing any proportion of dihydromorphine or its salts.
12. Morphine-N-oxide (also known as genomorphine) and any preparation, admixture, extract or other substance containing any proportion of morphine N-oxide.
13. Thebaine and its salts, and any preparation, admixture, extract or other substance containing any proportion of thebaine or its salts.
14. Benzylmorphine and its salts, and any preparation, admixture, extract or other substance containing any proportion of benzylmorphine or its salts.
15. Dihydrodesoxymorphine (also known as desomorphine) and its salts, and any preparation, admixture, extract or other substance containing any proportion of dihydrodesoxymorphine or its salts.
16. Pethidine and its salts and any preparation, admixture, extract or other substance containing any proportion of pethidine or its salts.
17. The isopropyl and other esters of 1-methyl-4-phenylpiperidine-4-carbolxylic acid (other than pethidine) and their salts and any preparation, admixture, extract or other substance containing any proportion of isopropyl or other esters of 1-methyl-4-phenylpiperidine-4-carboxylic acid or their salts.
18. Methyldihydromorphinone (also known as metopon) and its salts and any preparation, admixture, extract or other substance containing any proportion of methyldihydromorphinone or its salts..
19. Alphaprodine and its salts, and any preparation, admixture, extract or other substance containing any proportion of alphaprodine or its salts.
20. Methadone (also known as amidone) and its salts, and any preparation, admixture, extract or other substance containing any proportion of methadone or its salts.
21. Betaprodine and its salts, and any preparation, admixture, extract or other substance containing any proportion of betaprodine or its salts.
22. Hydroxypethidine and its salts, and any preparation, admixture, extract or other substance containing any proportion of hydroxypethidine or its salts.
23. Isomethadone (also known as isoamidone) and its salts, and any preparation, admixture, extract or other substance containing any proportion of isomethadone or its salts.
24. Ketobemidone and its salts, and any preparation, admixture, extract or other substance containing any proportion of ketobemidone or its salts.
25. Methadol and its salts and any preparation, admixture, extract or other substance containing any proportion of methadol or its salts.
26. a-methadol and its salts, and any preparation, admixture, extract or other substance containing any proportion of a-methadol or its salts.
27. b-methadol and its salts, and any preparation, admixture ,extract or other substance containing any proportion of b-methadol or its salts.
28. Methadyl acetate and its salts, and any preparation, admixture, extract or other substance containing any proportion of methadyl acetate or its salts.
29. a-acetylmethadol and its salts, and any preparation, admixture, extract or other substance containing any proportion of a-acetylmethadol or its salts.
30. b-acetylmethadol and its salts, and any preparation, admixture, extract or other substance containing any proportion of b-acetylmethadol or its salts.
31. Phenadoxone and its salts, and any preparation, admixture, extract or other substance containing any proportion of phenadoxone or its salts.
32. Betameprodine and its salts, and any preparation, admixture, extract or other substance containing any proportion of betameprodine or its salts.
33. Methorphinan, other than dextrorphan (that is to say levorphan and reacemorphan) and its salts, and any preparation, admixture, extract or other substance containing any proportion of methorphinan or its salts.
34. 3-methoxy-N-methylmorphinan, other than dextromethorphan,(that is to say, levomethorphan and racemethorphan), and its salts and any preparation, admixture, extract or other substance containing any proportion of 3-methyoxy-N-methylmorphinan or its salts.
35. Methyldesomorphine (6-methyl- desoxymorphine) and its salts, and any preparation, admixture, extract or other substance containing any proportion of methyldesomorphine or its salts.
36. 3-dimethylamino-1,1-di (2’-thienyl)-1- butene and its salts, and any preparation, admixture, extract or other substance containing any proportion of 3-dimethylamino-1,1-di(2’thienyl)-1-butene or its salts.
37. 3-ethylmethylamino-1, 1-di(2’-thienyl)-1-butene and its salts, and any preparation, admixture, extract or other substance containing any proportion of 3-ethylmethylamino-1, 1-di(2’thienyl)-1-butene or its salts.
38. 3-diethylyamino-1, 1-di-(2’-thienyl)-1-butene (diethylthiambutene) and its salts, and any preparation, admixture, extract or other substance containing any proportion of 3-diethylyamino-1, 1-di-(2’-thienyl)-1-butene or its Salts.
39. 4,4-diphenyl-6-dimethylamino-3-hexanone and its salts, and any preparation, admixture, extract or other substance containing any proportion of 4,4-diphenyl-6-dimethylamino-3-hexanone or its salts.
40. 4,4-diphenyl-6-piperidino-3-hepatanone and its salts, and any preparation, admixture, extract or other substance containing any proportion of 4,4-diphenyl-6-piperidino-3-hepatanone or its salts.
41. The esters of morphine (other than diacetylmorphine) ecgonine, dihydro-hydroxycodeinone, dihydrocodeinone, dihydromorphinone, acetyldihydro-codeinone and dihydromorphine and their respective salts, the ethers of morphine (other than benzylmorphine, methylmorphine, ethylmorphine and morpholinylethylmorphine) and their salts, and their salts, and the morphine-N-oxide derivatives and any other pentavalent nitrogen morphine derivatives, and any preparation, admixture, extract or other substance containing any proportion of any drug included in this paragraph.
42. 1:3-dimethyl-4-phenyl-4-propionyloxyhexamethyleneimine, its salts and any preparation, admixture, extract or other substance containing any proportion of 1:3-diamethyl-4-phenyl-4-propionyloxyhexamethylenieimine.
43. 3-hydroxy-N-phenethylmorphinan, its salts and any preparation, admixture, extract or other substance containing any proportion of 3-hydroxy-N-phenethylmorphinan.
44. 4-morpholino-2:2-dipenyl ethyl butyrate, its salts and any preparation, admixture, extract or other substance containing any proportion of 4-morpholino-2:2-dipenyl ethyl butyrate.
45. 4-dimethylamino-1:2-diphenyl-3-methyl-2-propionyloxybutane, its salts and any preparation, admixture, extract or other substance containing any proportion of 4-dimethylamino-1:2-diphenyl-3-methyl-2-propionyloxybutane.
46. Anileridine (1-[2-(p-aminophenyl)-ethyl]-4-phenylpiperidine-4-carbolyxic acid ethyl ester).
47. Etoxeridine (1-2[2-(2-hydroxyethoxy)-ethyl]-4-phenylpiperidine-4-carboxylic acid ethyl ester).
48. Dextromoramide, levomoramide and racemoramide [1-(3 methyl-4-morpholino-2 : diphenylbutyryl)-pyrrolidine].
49. Morpheridine[1-(2-morpholinoethyl)-4-phenylpiperidine-4-carboxylic acid ethyl ester].
50. Myrophine (myristyl ester of benzylmorphine).
51. Oxymorphone (dihydro-14-hydroxymorphinone).
52. Trimeperidine (1:2:5 trimethyl-4-phenyl-4-propionyloxy piperidine).
53. Benzethdine [ethyl 1 (2-benzoyloxyethyl)-4-phenylpiperidine-4-carboxylate).
54. Dimenoxadole (2-dimethylaminoethyl)-2-ethoxy-2 : 2 diphenylacetate).
55. Furethidine [ethyl 1 (2-tetrahydrofurfuryloxyethyl)-4-phenylpiperidine-4-carboxylate).
56. Norcodeine.
57. Normorphine.
58. Phenazocine [2’-hydroxy-5:9 dimethyl-2- (2-phenylethyl)-6:7-benzomorphan].
59. Allylprodine (3 allyl-1 methyl-4 phenyl-4 propionoxypiperidine).
60. Clonitazene (2-p-chlorobenzyl-1-1-(2-diethylamnoethyl)-5-nitrobenzimidazole).
61. Diphenoxylate [ethyl 1-(3-cyano-3:3 diphenylpropyl)-4-phenylpiperidine-4-carboxylate].
62. Etonitazine [1-(2-diethylaminoethyl)-2-p-ethoxybenzyl-5-nitrobenzimidzole].
63. Hydromorphinol (14-hydroxydihydromorphine).
64. Levophenacylmorphan [(-)-3 hydroxy-N-phenacylmorphinan].
65. Metazocine (2’-hydroxy-2:5:9-trimethyl-6: 7-benzomorphan).
66. Diampromide (N-[2-(N-methylphenethylamino)-propyl] propionanilide).
67. Norlevorphanol [(-)]-3 hydroxymorphinan].
68. Phenampromide [N-(1-methyl-2-piperidincethyl) propionanilide].
69. Phenoperidine [ethyl 1–(3-hydroxy-3-phenylpropyl)-4-phenylpiperidine-4-carboxylate].
70. Piminodine [ethyl-(3-anilinopropyl)-4-phenylpiperidine-4-carboxylate].
71. Nicocodine.
72. Noracymethadol (oe-dl-3 acetoxy-6 methylamino-4:4 diphenylheptane).
73. Acetorphine.
74. Etorphine.
75. Fentanyl
76. Piritramide.
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 2922.29.10: 5-nitro-2-n-propoxyaniline, 2922.29.90: Other, 2912.41.00: Vanillin(4-hydroxy-3-ethoxybenzaldehyde), 2915.70.00: Palmitic acid, stearic acid, their salts and esters and 2933.53.00: Allobarbital (inn),amobarbital (inn),barbital (inn), butalbital (inn), butobarbital, clobarbital (inn), methylphenobarbital (inn), pentobarbital (inn),phenobarbital (inn),secbutabarbital (inn), secobarbital (inn) and vinylbital (inn); salts there
The measure came into effect on 01 July 1991
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 01 July 1991
- Publication where the measure is specified
- Statutory Instrument 150 of 1991
- Regulation where the measure is specified
- Medicines and Allied Substances Control (General) Regulations, 1991
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not specified in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 72A. (1) Any person who wishes to
(a) import a psychotropic substance shall submit an application to the Director-General in Form M.C. 10A;
(b) export a psychotropic substance shall submit an application to the Director-General in Form M.C. 10B.
(2) Any person who imports or exports a psychotropic substance shall, for every import and export, as the case may be, whether such import or export consists of one or more substances, obtain a separate licence from the Authority for such importation or exportation.
(3) An import or export licence granted by the Authority shall state—
(a) the name and address of the importer or exporter, as the case may be;
(b) the international non-proprietary name of the psychotropic substance or if there is no such name, the appropriate name set out in Part I of the Eighth A Schedule;
(c) the quantity to be exported or imported;
(d) the pharmaceutical form;
(e) the period within which the import or export shall be effected;
(f) where the substance is imported or exported in the form of a preparation, the name of the preparation;
(4) An export licence shall state—
(a) the number and date of the import authorization; and
(b) the authority by whom it is issued.
(5) No export licence shall be granted in respect of a psychotropic substance by the Authority unless the exporter produces to the satisfaction of the Authority proof of an import authorization issued by a competent authority of the importing country confirming the approval of the proposed importation.
(6) A copy of the export licence shall accompany each consignment of a psychotropic substance, which is to be exported.
(7) Where any psychotropic substance is imported into Zimbabwe, the Director—General shall return authorization of the government of the exporting country and shall endorse on such authorization the amount of such substance, which has been actually imported.
(8) No psychotropic substance, which is in transit through Zimbabwe being exported from a destination outside Zimbabwe to another destination, shall be permitted to pass through Zimbabwe unless a copy of the export authorization is presented to and approved by the Director-General.
(9) Every consignment of a psychotropic substance whether imported or exported shall be accompanied by an export licence or similar authorization.
(10) Any consignment referred to in subsection (9) which is not accompanied by an export licence or similar authorization shall be detained by a customs officer until such licence or authorization is presented to and approved by the Director-General.
(11) No person shall mislabel any psychotropic substance intended for export.
(12) No psychotropic substance shall be imported or exported by ordinary or registered letter post.
(13) A licence granted by the Authority in term of subsection (1) shall –
(a) in the case of an import licence, be in Form M.C. 27;
(b) in the case of an export licence, be in Form M.C. 28. - Reference of the measure
- Art 72A (3)
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 2922.29.10 5-nitro-2-n-propoxyaniline No 2922.29.90 Other No 2912.41.00 Vanillin(4-hydroxy-3-ethoxybenzaldehyde) No 2915.70.00 Palmitic acid, stearic acid, their salts and esters No 2933.53.00 Allobarbital (inn),amobarbital (inn),barbital (inn), butalbital (inn), butobarbital, clobarbital (inn), methylphenobarbital (inn), pentobarbital (inn),phenobarbital (inn),secbutabarbital (inn), secobarbital (inn) and vinylbital (inn); salts there No - Description
- Psychotropic substance
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 2933.53.00: Allobarbital (inn),amobarbital (inn),barbital (inn), butalbital (inn), butobarbital, clobarbital (inn), methylphenobarbital (inn), pentobarbital (inn),phenobarbital (inn),secbutabarbital (inn), secobarbital (inn) and vinylbital (inn); salts there
The measure came into effect on 01 July 1991
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 01 July 1991
- Publication where the measure is specified
- Statutory Instrument 150 of 1991
- Regulation where the measure is specified
- Medicines and Allied Substances Control (General) Regulations, 1991
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not specified in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 72B. (1) Any person who exports a psychotropic substance set out in Part II of the Eighth A Schedule shall state in a declaration in Form M.C. 29, in triplicate, the following information –
(a) the names and addresses of the exporter and importer;
(b) the international non-proprietary name of the substance and if there is no international non-proprietary name, the designation of the substance in Part II of the Eighth A Schedule;
(c) the quantity and pharmaceutical form in which the substance is exported and if the substance is in the form of a preparation, the name of the preparation, if any;
(d) the date of dispatch;
(2) Every exporter shall –
(a) furnish the Authority with two copies of the declaration;
(b) attach the third copy of the declaration to the consignment being exported.
(3) Upon receipt of the copies of a declaration in terms of subsection (2) the Director-General shall, within ninety days, send one copy by registered mail, to the competent authority of the importing country requesting such authority to return the receipt thereof.
(4) Every importer shall, upon receipt of any substance set out in Part II of the Eighth A Schedule; send a copy of the consignment, duly endorsed, to the Director-General.
(5) No exporter of any psychotropic substance set out in Part II of the Eighth A Schedule shall export such substance to a bank - Reference of the measure
- Art 72 B(4)
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 2933.53.00 Allobarbital (inn),amobarbital (inn),barbital (inn), butalbital (inn), butobarbital, clobarbital (inn), methylphenobarbital (inn), pentobarbital (inn),phenobarbital (inn),secbutabarbital (inn), secobarbital (inn) and vinylbital (inn); salts there No - Description
- Amobarbital
Cyclobarbital
Pentobarbital
Secobarbital
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
-
Applied by Zimbabwe on the entire world for 3002.10.00: Antisera, other blood fractions and immunological products, whether or not modified or obtained by means of biotechnological processes, 3002.90.00: Other, 3004.90.00: - Other and 2933.53.00: Allobarbital (inn),amobarbital (inn),barbital (inn), butalbital (inn), butobarbital, clobarbital (inn), methylphenobarbital (inn), pentobarbital (inn),phenobarbital (inn),secbutabarbital (inn), secobarbital (inn) and vinylbital (inn); salts there
The measure came into effect on 01 July 1991
Non-Tariff Measure
- NTM classification
- B859: Traceability requirements, n.e.s.
- Date when the measure came into force
- 01 July 1991
- Publication where the measure is specified
- Statutory Instrument 150 of 1991
- Regulation where the measure is specified
- Medicines and Allied Substances Control (General) Regulations, 1991
- Country/Region applying the measure
- Zimbabwe
- The rationale of the measure
- Not specified in the regulations
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 72F. (1) Any person who is authorized or licensed to manufacture or supply a psychotropic substance set out in Parts I and II of the Eighth A Schedule or who imports or exports such substance shall keep a register and shall enter therein, in chronological sequence, true particulars with respect to such substance—
(a) every quantity of such substance manufactured by him;
(b) every quantity of such substance acquired by him;
(c) every quantity of such substance supplied y him;
(d) every quantity of such substance used by him;
(e) in respect of each acquisition and disposal of such substance details of the quantity, the date, the supplier and the person to whom the substance is supplied;
and the provisions of section 42 of the Dangerous Drugs Regulations, 1975, shall apply, mutatis mutandis.
(2) Subsection (1) shall apply to any hospital, clinic, dispensary, wholesaler or similar institution administered by the State.
(3) Every manufacturer, importer and exporter of a substance set out in Parts II and III of the Eighth A Schedule shall keep a record showing the quantities of such substance manufactured, imported or exported, as the case may be.
(4) The records required to be kept in terms of subsections (1) and (3) shall be kept for a period of five years. - Reference of the measure
- Art 72F
- Measure also domestic
- Yes
Products affected by the measure.
Code Product Partial coverage Partial coverage indication Date in Date out 3002.10.00 Antisera, other blood fractions and immunological products, whether or not modified or obtained by means of biotechnological processes No 3002.90.00 Other No 3004.90.00 - Other No 2933.53.00 Allobarbital (inn),amobarbital (inn),barbital (inn), butalbital (inn), butobarbital, clobarbital (inn), methylphenobarbital (inn), pentobarbital (inn),phenobarbital (inn),secbutabarbital (inn), secobarbital (inn) and vinylbital (inn); salts there No - Description
- Amphetamine
Dexamphetamine
Methamphetamine
Methylphenidate
Phencyclidine
Amobarbital
Cyclobarbital
Pentobarbital
Secobarbital
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world - Description
- All countries
B859: Traceability requirements, n.e.s.
