FDA NDC Directory · JSON-LD · Markdown

Prazosin Hydrochloride

NDC 68788-8742 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210971
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (2 mg/1)
Marketing started20240923
Package count4

External sources

Source: openFDA. Public-domain (CC0).