FDA NDC Directory · JSON-LD · Markdown

Buprenorphine

NDC 0228-3156 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090819
Dosage form / routeTABLET · SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (2 mg/1)
Marketing started20150219
Package count1

External sources

Source: openFDA. Public-domain (CC0).