FDA NDC Directory · JSON-LD · Markdown

Prazosin Hydrochloride

NDC 70010-084 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214608
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (1 mg/1)
Marketing started20220103
Package count2

External sources

Source: openFDA. Public-domain (CC0).