FDA NDC Directory · JSON-LD · Markdown

Prochlorperazine

NDC 54348-989 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePROCHLORPERAZINE
Labeler / ManufacturerPharmPak, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040268
Dosage form / routeTABLET · ORAL
Active ingredientsPROCHLORPERAZINE MALEATE (5 mg/1)
Marketing started20190711
Package count1

External sources

Source: openFDA. Public-domain (CC0).