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Fluphenazine Hydrochloride

NDC 43598-034 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDr. Reddys Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214534
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUPHENAZINE HYDROCHLORIDE (1 mg/1)
Marketing started20210215
Package count1

External sources

Source: openFDA. Public-domain (CC0).