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Fluphenazine Hydrochloride

NDC 0904-7157 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA089743
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUPHENAZINE HYDROCHLORIDE (1 mg/1)
Marketing started19880825
Package count1

External sources

Source: openFDA. Public-domain (CC0).