FDA NDC Directory · JSON-LD · Markdown

Buprenorphine

NDC 58118-4459 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerClinical Solutions Wholesale, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201760
Dosage form / routeTABLET · SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (2 mg/1)
Marketing started20160217
Package count1

External sources

Source: openFDA. Public-domain (CC0).