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Pentazocine and naloxone

NDC 0591-0395 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePentazocine hydrochloride and naloxone hydrochloride
Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074736
Dosage form / routeTABLET · ORAL
Active ingredientsNALOXONE HYDROCHLORIDE (.5 mg/1)
PENTAZOCINE HYDROCHLORIDE (50 mg/1)
Marketing started19970521
Package count1

External sources

Source: openFDA. Public-domain (CC0).