FDA NDC Directory · JSON-LD · Markdown

CHLORPROMAZINE HYDROCHLORIDE

NDC 60687-452 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA209755
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (100 mg/1)
Marketing started20190516
Package count1

External sources

Source: openFDA. Public-domain (CC0).