FDA NDC Directory · JSON-LD · Markdown

Buprenorphine

NDC 67296-2173 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRedpharm Drug
Marketing categoryAbbreviated NDA (generic) · App ANDA201760
Dosage form / routeTABLET · SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (8 mg/1)
Marketing started20160217
Package count1

External sources

Source: openFDA. Public-domain (CC0).