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Last update 24 Feb 2026
Ceftriaxone Sodium/Sulbactam sodium
Last update 24 Feb 2026
Overview
Basic Info
Drug Type Small molecule drug |
Synonyms Ceftriaxone Sodium and Sulbactam Sodium, Ceftriaxone Sodium and Tazobactam Sodium, 头孢曲松钠舒巴坦钠 |
Target |
Action inhibitors |
Mechanism PBPs inhibitors(Bacterial penicillin-binding protein inhibitors), β-lactamase inhibitors(Beta Lactamase inhibitors), Cell wall inhibitors |
Therapeutic Areas |
Active Indication |
Inactive Indication- |
Originator Organization |
Inactive Organization- |
License Organization- |
Drug Highest PhaseApproved |
First Approval Date China (28 Jan 2011), |
Regulation- |
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Structure/Sequence
Molecular FormulaC18H20N8NaO8S3 |
InChIKeyKFQRYHQOZUTRQJ-BBJOQENWSA-N |
CAS Registry104376-79-6 |
View All Structures (2)
Related
4
Clinical Trials associated with Ceftriaxone Sodium/Sulbactam sodiumNCT04202068
A Study Evaluating Efficacy and Safety of Ceftriaxone Sodium and Sulbactam Sodium for Injection in the Treatment of Uncomplicated Urogenital Gonorrhea
CTR20150336
注射用头孢曲松钠舒巴坦钠（2:1）治疗血液科细菌感染患者的开放式、多中心IV期临床试验
[Translation] An open, multicenter phase IV clinical trial of ceftriaxone sodium and sulbactam sodium for injection (2:1) in the treatment of patients with hematological bacterial infections
CTR20132092
“注射用头孢曲松钠舒巴坦钠（2:1）”治疗儿科急性细菌性感染的多中心、开放、非对照Ⅳ期临床研究
[Translation] A multicenter, open, non-controlled phase IV clinical study of "Ceftriaxone Sodium and Sulbactam Sodium for Injection (2:1)" for the treatment of acute bacterial infections in children
100 Clinical Results associated with Ceftriaxone Sodium/Sulbactam sodium
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100 Translational Medicine associated with Ceftriaxone Sodium/Sulbactam sodium
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100 Patents (Medical) associated with Ceftriaxone Sodium/Sulbactam sodium
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100 Deals associated with Ceftriaxone Sodium/Sulbactam sodium
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External Link
| KEGG | Wiki | ATC | Drug Bank |
|---|---|---|---|
| - | - | - |
R&D Status
10 top approved records. to view more data
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| Indication | Country/Location | Organization | Date |
|---|---|---|---|
| Bacterial Infections | China | 28 Jan 2011 |
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Clinical Result
Clinical Result
Indication
Phase
Evaluation
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