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Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate

NDC 58118-8020 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerClinical Solutions Wholesale, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207000
Dosage form / routeTABLET · SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (8 mg/1)
NALOXONE HYDROCHLORIDE DIHYDRATE (2 mg/1)
Marketing started20171213
Package count1

External sources

Source: openFDA. Public-domain (CC0).