FDA NDC Directory · JSON-LD · Markdown

Naltrexone Hydrochloride

NDC 42291-632 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAvKARE
Marketing categoryAbbreviated NDA (generic) · App ANDA075274
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNALTREXONE HYDROCHLORIDE (50 mg/1)
Marketing started20150326
Marketing ended20280630
Package count2

External sources

Source: openFDA. Public-domain (CC0).