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Chlorthalidone

NDC 83980-062 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerIpca Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209162
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORTHALIDONE (50 mg/1)
Marketing started20260921
Package count4

External sources

Source: openFDA. Public-domain (CC0).