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Prazosin Hydrochloride

NDC 59651-271 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA213052
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (1 mg/1)
Marketing started20230331
Package count2

External sources

Source: openFDA. Public-domain (CC0).