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Buprenorphine and Naloxone

NDC 0378-8765 · HUMAN PRESCRIPTION DRUG · FILM

Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211785
Dosage form / routeFILM · BUCCAL SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (2 mg/1)
NALOXONE HYDROCHLORIDE DIHYDRATE (.5 mg/1)
Marketing started20200417
Package count1

External sources

Source: openFDA. Public-domain (CC0).