FDA NDC Directory · JSON-LD · Markdown

NALTREXONE HYDROCHLORIDE

NDC 71610-919 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namenaltrexone hydrochloride
Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076264
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNALTREXONE HYDROCHLORIDE (50 mg/1)
Marketing started20020322
Package count1

External sources

Source: openFDA. Public-domain (CC0).