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Prazosin Hydrochloride

NDC 70518-1443 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameprazosin hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA072575
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (5 mg/1)
Marketing started20180928
Package count1

External sources

Source: openFDA. Public-domain (CC0).