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Buprenorphine hydrochloride

NDC 68083-696 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA221145
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (.324 mg/mL)
Marketing started20261015
Package count1

External sources

Source: openFDA. Public-domain (CC0).