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Chlorpromazine Hydrochloride

NDC 70518-4142 · HUMAN PRESCRIPTION DRUG · TABLET, SUGAR COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA214827
Dosage form / routeTABLET, SUGAR COATED · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (200 mg/1)
Marketing started20240717
Package count1

External sources

Source: openFDA. Public-domain (CC0).