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perphenazine

NDC 70771-1043 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA205232
Dosage form / routeTABLET · ORAL
Active ingredientsPERPHENAZINE (8 mg/1)
Marketing started20200716
Package count3

External sources

Source: openFDA. Public-domain (CC0).