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Buprenorphine and Naloxone

NDC 0378-8767 · HUMAN PRESCRIPTION DRUG · FILM

Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207607
Dosage form / routeFILM · BUCCAL SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (8 mg/1)
NALOXONE HYDROCHLORIDE DIHYDRATE (2 mg/1)
Marketing started20190220
Package count1

External sources

Source: openFDA. Public-domain (CC0).