Ceftriaxone Sodium

NDC 0409-7338 · Hospira, Inc

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

Generic nameCeftriaxone Sodium

Dosage formINJECTION, POWDER, FOR SOLUTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)CEFTRIAXONE SODIUM

Strength500 mg/1

Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]

Marketing categoryANDA

Packages

0409-7338-20 — 10 VIAL, SINGLE-USE in 1 CARTON (0409-7338-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7338-21)

0409-7338-01 — 10 VIAL, SINGLE-USE in 1 CARTON (0409-7338-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7338-11)

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.

0264-3153 — CEFTRIAXONE, 0264-3155 — CEFTRIAXONE, 0338-5002 — Ceftriaxone Sodium, 0338-5003 — Ceftriaxone Sodium, 0409-7332 — Ceftriaxone Sodium, 0409-7333 — Ceftriaxone Sodium, 0409-7334 — Ceftriaxone Sodium, 0409-7335 — Ceftriaxone Sodium, 0409-7336 — Ceftriaxone Sodium, 0409-7337 — 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, 44567-702 — 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.