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ChlorproMAZINE Hydrochloride

NDC 63304-083 · HUMAN PRESCRIPTION DRUG · TABLET, SUGAR COATED

Generic nameChlorproMAZINE
Labeler / ManufacturerSun Pharmaceutical Industries Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA214256
Dosage form / routeTABLET, SUGAR COATED · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (200 mg/1)
Marketing started20201118
Package count2

External sources

Source: openFDA. Public-domain (CC0).