FDA NDC Directory · JSON-LD · Markdown

Naltrexone Hydrochloride

NDC 68094-853 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namenaltrexone Hydrochloride
Labeler / ManufacturerPrecision Dose Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075274
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNALTREXONE HYDROCHLORIDE (50 mg/1)
Marketing started20141029
Package count3

External sources

Source: openFDA. Public-domain (CC0).