Ceftriaxone

NDC 44567-702 · WG Critical Care, LLC

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameCeftriaxone

Dosage formINJECTION, POWDER, FOR SOLUTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)CEFTRIAXONE SODIUM

Strength2 g/1

Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]

Marketing categoryANDA

Packages

44567-702-95 — 25 VIAL in 1 CARTON (44567-702-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

44567-702-25 — 25 VIAL in 1 CARTON (44567-702-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

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.

0409-7338 — Ceftriaxone Sodium, 0781-3206 — Ceftriaxone Sodium, 0781-3207 — Ceftriaxone Sodium, 0781-3208 — Ceftriaxone Sodium, 0781-3209 — Ceftriaxone Sodium, 0781-3210 — Ceftriaxone Sodium, 25021-106 — ceftriaxone, 25021-107 — ceftriaxone, 44567-700 — Ceftriaxone, 44567-701 — 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, 60505-6151 — Ceftriaxone Sodium, 60505-6152 — Ceftriaxone Sodium, +34 more

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