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fluphenazine hydrochloride

NDC 62135-415 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215141
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUPHENAZINE HYDROCHLORIDE (1 mg/1)
Marketing started20220101
Package count1

External sources

Source: openFDA. Public-domain (CC0).