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Doxazosin

NDC 0904-5522 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA075580
Dosage form / routeTABLET · ORAL
Active ingredientsDOXAZOSIN MESYLATE (1 mg/1)
Marketing started20110714
Package count1

External sources

Source: openFDA. Public-domain (CC0).