Prasugrel

NDC 65862-829 · Aurobindo Pharma Limited

Generic namePrasugrel

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)PRASUGREL HYDROCHLORIDE

Strength5 mg/1

Pharmacologic classDecreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]

Marketing categoryANDA

Packages

65862-829-03 — 3 BLISTER PACK in 1 CARTON (65862-829-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-829-10)

65862-829-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-829-30)

FDA lists these products with the same active ingredient.

0378-5185 — Prasugrel, 0378-5186 — Prasugrel, 0713-0881 — Prasugrel Hydrochloride, 0713-0882 — Prasugrel Hydrochloride, 16729-272 — Prasugrel, 16729-273 — Prasugrel, 29300-301 — Prasugrel, 29300-302 — Prasugrel, 43817-239 — PRASUGREL, 43817-240 — PRASUGREL, 51407-444 — Prasugrel, 51407-445 — Prasugrel, 60505-4642 — PRASUGREL, 60505-4643 — PRASUGREL, 60505-4856 — PRASUGREL, 60687-883 — Prasugrel, 63629-4829 — Prasugrel, 65162-001 — Prasugrel, 65162-002 — Prasugrel, 65862-830 — Prasugrel

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.