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CHLORTHALIDONE CHLORTHALIDONE

NDC 46708-677 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCHLORTHALIDONE
Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216262
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORTHALIDONE (50 mg/1)
Marketing started20220829
Package count3

External sources

Source: openFDA. Public-domain (CC0).