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Buprenorphine Hydrochloride

NDC 0143-9246 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076931
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (.324 mg/mL)
Marketing started20050525
Package count1

External sources

Source: openFDA. Public-domain (CC0).