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Chlorpromazine Hydrochloride

NDC 0832-6021 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA084115
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (200 mg/1)
Marketing started20110803
Package count3

External sources

Source: openFDA. Public-domain (CC0).