<p> DESIGNATED ABATTOIRS</p><p>1. OKAHANDJA ABATTOIR No. 23; 2. OSHAKATI ABATTOIR No. 67; 3. OTAVI ABATTOIR No. 25; 4. WINDHOEK ABATTOIR No. 22; 5. MARIENTAL ABATTOIR No. 21; 6. KEETMANSHOOP ABATTOIR No. 20. 7. WITVLEI ABATTOIR No. 19.</p><p>DESIGNATED COUNTRIES</p><p>1.ANY COUNTRY WHICH IS A MEMBER STATE OF THE INTERNATIONAL ORGANISATION KNOWN AS THE EUROPEAN UNION. 2.SWITZERLAND. 3.NORWAY. 4.SPECIAL ADMINISTRATURE REGION OF HONG KONG.</p><p>DESIGNATED LABORATORIES</p><p>1.NATIONAL AND REFERENCE LABORATORIES OF THE EUROPEAN UNION 2.CENTRAL VETERINARY LABORATORY, NAMIBIA 3.ANALYTICAL AGRICULTURE LABORATORIES OF THE GOVERNMENT OF THE REPUBLIC OF NAMIBIA 4.LABORATORIES OF THE UNIVERSITY OF THE ORANGE FREE STATE, BLOEMFONTEIN, SOUTH AFRICA 5.LABORATORIES OF THE UNIVERSITY OF PRETORIA, PRETORIA, SOUTH AFRICA 6.LABORATORIES OF MEDUNSA UNIVERSITY, PRETORIA, SOUTH AFRICA 7.LABORATORIES OF THE COUNCIL FOR SCIENTIFIC AND INDUSTRIAL RESEARCH, PRETORIA, SOUTH AFRICA 8.LABORATORIES OF ONDERSTEPOORT VETERINARY INSTITUTE, PRETORIA, SOUTH AFRICA 9.LABORATORIES OF THE SOUTH AFRICAN BUREAU OF STANDARDS 10.TOBACCO RESEARCH BOARD, HARARE, ZIMBABWE AGRICULTURE, WATER AND RURAL DEVELOPMENT.</p><p>DECLARATION OF PROHIBITED, GROUP I, GROUP II AND GROUP III SUBSTANCES AND DETERMINATION OF WITHDRAWAL TIMES FOR PURPOSES OF THE PREVENTION OF UNDESIRABLE RESIDUE IN MEAT ACT, 1991.</p><p>UNDER SECTION 2 OF THE PREVENTION OF UNDERSIRABLE RESIDUE IN MEAT ACT, 1991 (ACT 21 OF 1991), I HEREBY DECLARE THE PRODUCTS SET OUT IN ANNEXURES I, II, III AND IV OF THE SCHEDULE AS PROHIBITED SUBSTANCES, GROUP II SUBSTANCES, GROUP III SUBSTANCES AND GROUP I SUBSTANCES RESPECTIVELY, AND DETERMINE THE RESPECTIVE WITHDRAWAL TIMES OF SUCH GROUP II SUBSTANCES AND GROUP III SUBSTANCES ACCORDINGLY</p><p>MINISTER OF AGRICULTURE,</p><p>WATER AND RURAL DEVELOPMENT. WINDHOEK………………….</p><p>SCHEDULE</p><p>TABLE I</p><p>PROHIBITED SUBSTANCES (a) SPECIFIED PRODUCTS PRODUCT ACTIVE INGREDIENT COMPOSITION PRESENTATION Compudose Oestradiol – 17 –beta Implant Compudose 100 Oestradiol 17 beta Implant F- To Testosterone and oestradiol Implant Gannamax – S Progesterone and oestradiol benzoate Implant M-PO Progesterone and oestradiol Implant Neoplix – F Testosterone and oestradiol Implant Neoplix – M Progesterone and oestradiol Implant Synovex – C Oestradiol benzoate and progesterone Implant Synovex – H Oestradiol benzoate and testosterone Implant Synovex plus Oestradiol benzoate and trenbolone acetate Implant Synovex – S Oestradiol benzoate and progesterone Implant Coopers revalor Trenbolone acetate and oestradiol – 17 beta Implant Ralgro Zeranol Implant Ralgro Sheep/Ostrich Zeranol Implant Ralgro – Super Zeranol Implant Revalor – H Trenbolone acetate and oestradiol – 17 beta Implant Revalor – S Trenbolone acetate and oestradiol – 17 beta Oestradiol Implant MGA 100 Melengestrol acetate Premix (b) OTHER PRODUCTS Any other product (except a group I substance) which is used in connection with animals for purposes of fattening and contains the above-mentioned or similar active ingredients. TABLE II</p><p>GROUP II SUBSTANCES PRODUCT/GROUP ACTIVE INGREDIENT OR PRESENTATION/ WITHDRAWAL TIMES(4) ACTION ADMINISTRATION Antibiotics (1) antibiotic Food or drinking water beta-agonist group (2) β adrenoreceptor action Injection In all cases as assigned to Chronogest sponge Flugestone acetate Intra-uterine sponge the product during Crestar (3) Norgestomet Implant registration under the laws ECP (1) Estradiol cypionate Inject referred to in Section 2 of Eazi-Breed B+G Progesterone Intra – uterine device the Act Metrijet Ethinyloestradiol Intra - uterine Nymphalon(1) Progesterone Injection Ovakron ESP Flugestone acetate Intra – uterine sponge Repromap Medroxyprogesterone acetate Intra – uterine sponge Utocyl Ethinyloestradiol Intra – uterine pessary</p><p>(1) For therapeutic treatment of designated animals. (2) For tocolysis in prescribed animals.(see max withdrawal time = subregulation 2.(2)(iii) ) (3) For synchronisation of oestrus in designated animals only (4) See also regulation 2 of the Regulations promulgated in terms of the Prevention of undesirable Residue in Meat Act, 1991(Act 21 0f 19991)</p><p>TABLE III</p><p>GROUP III SUBSTANCES</p><p>ACTIVE INGREDIENT COMPOSITION RESPECTIVE WITHDRAWAL TIMES*</p><p>Acepromazine maleate Five days Acetyl Promazine Five days Propionyl promazine Five days Phenylbutazone Fifteen days See also regulation 2 of the Regulations promulgated in terms of the Prevention of Undesirable Residue in Meat Act, 1991 (Act 21 of 1991).</p><p>TABLE IV</p><p>GROUP I SUBSTANCES (1) ACTIVE INGREDIENT COMPOSITION PRESENTATION OR GROUP OF SUBSTANCES Chloramphenicol Inject Chloroform Any Chlorpromazine Any Colchicine Inject Dapsone Inject Dimetridazole Any Furazolidone Any Metronidizole Any Nitrofuran Any Ronidazole Any Bovine Somatrotropin Inject Beta agonist group Any except GP II substances (1) In addition also see the definition of section I of the Prevention of Undesirable Residue in Meat Act,1991 (Act 21 of 1991)</p>