FDA NDC Directory · JSON-LD · Markdown

NALTREXONE HYDROCHLORIDE

NDC 70518-2718 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA090356
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNALTREXONE HYDROCHLORIDE (50 mg/1)
Marketing started20200501
Package count1

External sources

Source: openFDA. Public-domain (CC0).