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Chlorpromazine

NDC 46708-736 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA217350
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (25 mg/1)
Marketing started20230720
Package count3

External sources

Source: openFDA. Public-domain (CC0).