FDA NDC Directory · JSON-LD · Markdown

prochlorperazine maleate

NDC 59651-773 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218734
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPROCHLORPERAZINE MALEATE (5 mg/1)
Marketing started20250908
Package count1

External sources

Source: openFDA. Public-domain (CC0).