FDA NDC Directory · JSON-LD · Markdown

Chlorthalidone

NDC 72789-359 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA089286
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORTHALIDONE (50 mg/1)
Marketing started20231027
Package count2

External sources

Source: openFDA. Public-domain (CC0).