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Chlorthalidone

NDC 70518-3954 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA213412
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORTHALIDONE (25 mg/1)
Marketing started20231211
Package count1

External sources

Source: openFDA. Public-domain (CC0).