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PROCHLORPERAZINE MALEATE

NDC 69452-310 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameProchlorperazine Maleate
Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217478
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPROCHLORPERAZINE MALEATE (10 mg/1)
Marketing started20230913
Package count2

External sources

Source: openFDA. Public-domain (CC0).