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prazosin hydrochloride

NDC 76420-526 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerASCLEMED USA INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215697
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (5 mg/1)
Marketing started20230103
Package count6

External sources

Source: openFDA. Public-domain (CC0).