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Fluphenazine Hydrochoride

NDC 70518-4691 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namefluphenazine hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA218283
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUPHENAZINE HYDROCHLORIDE (10 mg/1)
Marketing started20260703
Package count1

External sources

Source: openFDA. Public-domain (CC0).