FDA NDC Directory · JSON-LD · Markdown

PROCHLORPERAZINE MALEATE

NDC 69315-265 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218912
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPROCHLORPERAZINE MALEATE (5 mg/1)
Marketing started20250625
Package count1

External sources

Source: openFDA. Public-domain (CC0).