Ceftriaxone Sodium

NDC 0409-7335 · 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

Strength2 g/1

Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]

Marketing categoryANDA

Packages

0409-7335-20 — 10 VIAL, SINGLE-USE in 1 CARTON (0409-7335-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7335-21)

0409-7335-03 — 10 VIAL, SINGLE-USE in 1 CARTON (0409-7335-03) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7335-13)

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.

0143-9857 — Ceftriaxone, 0143-9858 — Ceftriaxone, 0143-9859 — ceftriaxone, 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, 0409-7336 — Ceftriaxone Sodium, 0409-7337 — Ceftriaxone Sodium, 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, +34 more

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