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candesartan cilexetil and hydrochlorothiazide

NDC 70771-1326 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203466
Dosage form / routeTABLET · ORAL
Active ingredientsCANDESARTAN CILEXETIL (32 mg/1)
HYDROCHLOROTHIAZIDE (12.5 mg/1)
Marketing started20180414
Package count5

External sources

Source: openFDA. Public-domain (CC0).