FDA NDC Directory · JSON-LD · Markdown

CHLORTHALIDONE

NDC 64980-304 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206904
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORTHALIDONE (50 mg/1)
Marketing started20170517
Marketing ended20270131
Package count1

External sources

Source: openFDA. Public-domain (CC0).