FDA NDC Directory · JSON-LD · Markdown

Prazosin Hydrochloride

NDC 0093-4067 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071745
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (1 mg/1)
Marketing started20070222
Package count2

External sources

Source: openFDA. Public-domain (CC0).