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Chlorthalidone

NDC 67877-697 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213412
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORTHALIDONE (50 mg/1)
Marketing started20200213
Package count4

External sources

Source: openFDA. Public-domain (CC0).