Skip to main content

Ceftriaxone Sodium

NDC 67184-1007 · Qilu Pharmaceutical Co., Ltd.

Generic nameCeftriaxone Sodium
Dosage formINJECTION, POWDER, FOR SOLUTION
RouteINTRAMUSCULAR, INTRAVENOUS
Active ingredient(s)CEFTRIAXONE SODIUM
Strength1 g/1
Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]
Marketing categoryANDA

Packages

67184-1007-1 — 10 VIAL, SINGLE-USE in 1 CARTON (67184-1007-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-3838 — Ceftriaxone Sodium, 60505-6148 — Ceftriaxone Sodium, 60505-6149 — Ceftriaxone Sodium, 60505-6150 — Ceftriaxone Sodium, 60505-6151 — Ceftriaxone Sodium, 60505-6152 — Ceftriaxone Sodium, 63323-346 — Ceftriaxone, 66288-6100 — Ceftriaxone Sodium, 67184-1005 — Ceftriaxone Sodium, 67184-1006 — Ceftriaxone Sodium, 67184-1008 — Ceftriaxone Sodium, 70518-2499 — Ceftriaxone Sodium, 71205-545 — Ceftriaxone Sodium, 71205-593 — Ceftriaxone, 71205-710 — Ceftriaxone Sodium, 72572-061 — Ceftriaxone, 72572-062 — Ceftriaxone, 76420-596 — Ceftriaxone Sodium, 82804-066 — Ceftriaxone Sodium, 85766-069 — Ceftriaxone Sodium, +34 more

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