FDA NDC Directory · JSON-LD · Markdown

Prazosin Hydrochloride

NDC 0904-7020 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA210971
Dosage form / routeCAPSULE · ORAL
Active ingredientsPRAZOSIN HYDROCHLORIDE (1 mg/1)
Marketing started20181003
Package count1

External sources

Source: openFDA. Public-domain (CC0).