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Doxazosin

NDC 70771-1114 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208719
Dosage form / routeTABLET · ORAL
Active ingredientsDOXAZOSIN MESYLATE (4 mg/1)
Marketing started20170831
Package count4

External sources

Source: openFDA. Public-domain (CC0).