FDA NDC Directory · JSON-LD · Markdown

BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE

NDC 71335-1858 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA209069
Dosage form / routeTABLET · SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (8 mg/1)
NALOXONE HYDROCHLORIDE DIHYDRATE (2 mg/1)
Marketing started20210122
Package count10

External sources

Source: openFDA. Public-domain (CC0).