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Naltrexone Hydrochloride

NDC 68094-909 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPrecision Dose Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075274
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNALTREXONE HYDROCHLORIDE (50 mg/1)
Marketing started20240215
Marketing ended20280630
Package count2

External sources

Source: openFDA. Public-domain (CC0).