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Chlorpromazine hydrochloride

NDC 0641-1397 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA083329
Dosage form / routeINJECTION · INTRAMUSCULAR
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (25 mg/mL)
Marketing started19740725
Package count1

External sources

Source: openFDA. Public-domain (CC0).