bivalirudin

NDC 0781-3158 · Sandoz Inc

Generic namebivalirudin

Dosage formINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

RouteINTRAVENOUS

Active ingredient(s)BIVALIRUDIN

Strength250 mg/1

Pharmacologic classAnti-coagulant [EPC], Direct Thrombin Inhibitor [EPC], Thrombin Inhibitors [MoA]

Marketing categoryNDA AUTHORIZED GENERIC

Packages

0781-3158-95 — 10 VIAL, SINGLE-USE in 1 CARTON (0781-3158-95) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (0781-3158-94)

J0583 — Injection, bivalirudin, 1 mg Medicare Part B payment limit (ASP + 6%): $0.17

FDA lists these products with the same active ingredient.

16729-275 — bivalirudin, 42023-622 — Bivalirudin, 52958-034 — Bivalirudin, 55111-652 — Bivalirudin, 55150-210 — BIVALIRUDIN, 63323-562 — Bivalirudin, 67457-256 — bivalirudin, 70436-025 — bivalirudin, 70511-142 — Bivalirudin, 71288-427 — BIVALIRUDIN, 72572-035 — bivalirudin, 83634-400 — bivalirudin

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