Ceftriaxone Sodium

NDC 60505-6151 · Apotex Corp.

Generic nameCeftriaxone Sodium

Dosage formINJECTION, POWDER, FOR SOLUTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)CEFTRIAXONE SODIUM

Strength250 mg/1

Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]

Marketing categoryANDA

Packages

60505-6151-1 — 10 VIAL, SINGLE-USE in 1 CARTON (60505-6151-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

60505-6151-4 — 1 VIAL, SINGLE-USE in 1 CARTON (60505-6151-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

J0696 — Injection, ceftriaxone sodium, per 250 mg Medicare Part B payment limit (ASP + 6%): $0.40

FDA lists these products with the same active ingredient.

44567-701 — Ceftriaxone, 44567-702 — Ceftriaxone, 44567-703 — Ceftriaxone, 50090-0944 — Ceftriaxone Sodium, 50090-1875 — Ceftriaxone Sodium, 50090-2444 — Ceftriaxone Sodium, 50090-3838 — Ceftriaxone Sodium, 60505-6148 — Ceftriaxone Sodium, 60505-6149 — Ceftriaxone Sodium, 60505-6150 — Ceftriaxone Sodium, 60505-6152 — Ceftriaxone Sodium, 63323-346 — Ceftriaxone, 66288-6100 — Ceftriaxone Sodium, 67184-1005 — Ceftriaxone Sodium, 67184-1006 — Ceftriaxone Sodium, 67184-1007 — Ceftriaxone Sodium, 67184-1008 — Ceftriaxone Sodium, 70518-2499 — Ceftriaxone Sodium, 71205-545 — Ceftriaxone Sodium, 71205-593 — Ceftriaxone, +34 more

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