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Chlorthalidone

NDC 71205-592 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA207222
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORTHALIDONE (25 mg/1)
Marketing started20180528
Package count3

External sources

Source: openFDA. Public-domain (CC0).