FDA NDC Directory · JSON-LD · Markdown

prazosin hydrochloride

NDC 70518-3669 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215697
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (1 mg/1)
Marketing started20230303
Package count2

External sources

Source: openFDA. Public-domain (CC0).