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Naltrexone Hydrochloride

NDC 62135-242 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207905
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNALTREXONE HYDROCHLORIDE (50 mg/1)
Marketing started20170721
Package count3

External sources

Source: openFDA. Public-domain (CC0).