FDA NDC Directory · JSON-LD · Markdown

Chlorpromazine Hydrochloride

NDC 0527-2965 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212996
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsCHLORPROMAZINE HYDROCHLORIDE (200 mg/1)
Marketing started20210122
Package count2

External sources

Source: openFDA. Public-domain (CC0).