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PROCHLORPERAZINE MALEATE

NDC 68462-947 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGLENMARK PHARMACEUTICALS INC., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA216595
Dosage form / routeTABLET · ORAL
Active ingredientsPROCHLORPERAZINE MALEATE (10 mg/1)
Marketing started20250528
Package count2

External sources

Source: openFDA. Public-domain (CC0).