FDA NDC Directory · JSON-LD · Markdown

Chlorpromazine Hydrochloride

NDC 71656-101 · HUMAN PRESCRIPTION DRUG · CONCENTRATE

Labeler / ManufacturerSaptalis Pharmaceuticals, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA080983
Dosage form / routeCONCENTRATE · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (100 mg/mL)
Marketing started20260304
Package count1

External sources

Source: openFDA. Public-domain (CC0).