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Chlorpromazine Hydrochloride

NDC 70710-1850 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217275
Dosage form / routeINJECTION · INTRAMUSCULAR
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (25 mg/mL)
Marketing started20240329
Package count1

External sources

Source: openFDA. Public-domain (CC0).