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chlorpromazine hydrochloride

NDC 62135-421 · HUMAN PRESCRIPTION DRUG · TABLET, SUGAR COATED

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212630
Dosage form / routeTABLET, SUGAR COATED · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (25 mg/1)
Marketing started20220205
Package count1

External sources

Source: openFDA. Public-domain (CC0).