FDA NDC Directory · JSON-LD · Markdown

Prasugrel

NDC 60687-883 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA205888
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPRASUGREL HYDROCHLORIDE (10 mg/1)
Marketing started20250302
Package count1

External sources

Source: openFDA. Public-domain (CC0).