Label: OXIBENDAZOLE- oxibendazol powder
- NDC Code(s): 51927-5201-0
- Packager: Professional Compounding Centers of America
- This is a repackaged label.
- Source NDC Code(s): 52286-0002
- Category: BULK INGREDIENT - ANIMAL DRUG
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated January 12, 2023
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- Official Label (Printer Friendly)
- OXIBENDAZOLE (FOR VETERINARY USE ONLY)FOR PRESCRIPTION COMPOUNDING/RX ONLYPART: 30-5021CAS: 20559-55-1WARNING:HARMFUL BY INHALATION, SKIN CONTACT & IF SWALLOWED. WEAR PROTECTIVE GLOVES & FACE/EYE PROTECTION.Storage: STORE IN TIGHTLY CLOSED CONTAINER. STORE AT ROOM TEMPERATURE.
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INGREDIENTS AND APPEARANCE
OXIBENDAZOLE
oxibendazol powderProduct Information Product Type Item Code (Source) NDC:51927-5201(NDC:52286-0002) Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXIBENDAZOLE (UNII: 022N12KJ0X) (OXIBENDAZOLE - UNII:022N12KJ0X) OXIBENDAZOLE 1 kg in 1 kg Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51927-5201-0 1 kg in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 01/12/2023 Labeler - Professional Compounding Centers of America (047919147) Establishment Name Address ID/FEI Business Operations Professional Compounding Centers of America 047919147 repack
