FDA NDC Directory · JSON-LD · Markdown

Chlorpromazine Hydrochloride

NDC 0781-4027 · HUMAN PRESCRIPTION DRUG · CONCENTRATE

Labeler / ManufacturerSandoz, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214542
Dosage form / routeCONCENTRATE · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (30 mg/mL)
Marketing started20230331
Package count1

External sources

Source: openFDA. Public-domain (CC0).