MedPath

Teicoplanin

Generic Name
Teicoplanin
Drug Type
Small Molecule
Chemical Formula
C88H97Cl2N9O33
CAS Number
61036-62-2
Unique Ingredient Identifier
4U3D3YY81M

Overview

Teicoplanin is a glycopeptide antibiotic consisting of a mixture of several compounds, five major (named teicoplanin A2-1 through A2-5) and four minor (named teicoplanin RS-1 through RS-4). All teicoplanins share a same glycopeptide core, teicoplanin A3-1, but differ in the length and conformation of side chains attached to their β-D-glucosamine moiety.

Background

Teicoplanin is a glycopeptide antibiotic consisting of a mixture of several compounds, five major (named teicoplanin A2-1 through A2-5) and four minor (named teicoplanin RS-1 through RS-4). All teicoplanins share a same glycopeptide core, teicoplanin A3-1, but differ in the length and conformation of side chains attached to their β-D-glucosamine moiety.

Indication

For the treatment of bacterial infections caused by susceptible microorganisms.

Associated Conditions

  • Angina Pectoris
  • Anginal Pain
  • Bacteremia
  • Bloodstream Infections (BSI)
  • Bone and Joint Infections
  • Clostridium Difficile
  • Clostridium Difficile Infection (CDI)
  • Community Acquired Pneumonia (CAP)
  • Complicated Urinary Tract Infection
  • Infective Endocarditis (IE)
  • Lower Respiratory Tract and Lung Infections
  • Non-complicated Skin and Soft Tissue Infections
  • Nosocomial Pneumonia
  • Peritonitis
  • Skin and Soft Tissue Infections (SSTIs)
  • Urinary Tract Infection

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/02/10
Not Applicable
Not yet recruiting
2023/06/22
Phase 4
Recruiting
2020/04/30
Phase 4
Completed
2020/04/10
Phase 3
UNKNOWN
2019/11/25
Phase 1
Completed
2019/07/01
Phase 4
Terminated
2017/01/13
N/A
UNKNOWN
2016/01/11
Not Applicable
Recruiting
2013/12/23
Phase 4
Completed
2013/03/21
Phase 2
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
Teicoplanin for Injection
国药准字H20253100
化学药品
注射剂
1/8/2025
Teicoplanin for Injection
国药准字H20253606
化学药品
注射剂
3/11/2025
Teicoplanin for Injection
国药准字H20253762
化学药品
注射剂
4/1/2025
Teicoplanin for Injection
国药准字H20123376
化学药品
注射剂
10/17/2022
Teicoplanin for Injection
国药准字H20123375
化学药品
注射剂
10/17/2022
Teicoplanin for Injection
国药准字H20040387
化学药品
注射剂
4/9/2020
Teicoplanin for Injection
国药准字HJ20160586
化学药品
注射剂
8/1/2023
Teicoplanin for Injection
国药准字HJ20160587
化学药品
注射剂
8/1/2023
Teicoplanin for Injection
国药准字H20249218
化学药品
注射剂
10/29/2024
Teicoplanin for Injection
国药准字H20249206
化学药品
注射剂
10/29/2024

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.
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