FDA NDC Directory · JSON-LD · Markdown

PROCHLORPERAZINE MALEATE

NDC 69452-472 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameProchlorperazine Maleate
Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217478
Dosage form / routeTABLET · ORAL
Active ingredientsPROCHLORPERAZINE MALEATE (10 mg/1)
Marketing started20250131
Package count2

External sources

Source: openFDA. Public-domain (CC0).