FDA NDC Directory · JSON-LD · Markdown

Prazosin hydrochloride

NDC 70377-068 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerBiocon Pharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213406
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (5 mg/1)
Marketing started20230109
Package count1

External sources

Source: openFDA. Public-domain (CC0).