Antibiotic & Anti-infective

TeicoplaninThird Party Manufacturing in India

Looking to get Teicoplanin manufactured under your brand? Our WHO-GMP certified partner facilities support PCD franchise partners and global export opportunities structured across 25+ countries.

WHO-GMP Certified
Export Ready
PCD Franchise Available
CAS Number
61036-62-2
Drug Class
Glycopeptide antibiotic
Molecular Formula
C₈₈H₉₅Cl₂N₉O₃₃
Molecular Weight
1,877.7 g/mol
Grade Standards
IP, BP, EP
Therapeutic Category
Antibiotic & Anti-infective
MOQ
Contact us for MOQ — varies by strength and batch size
Dosage Forms
Injection (Lyophilized Powder)

Mechanism of Action

Teicoplanin is a glycopeptide antibiotic that works by inhibiting bacterial cell wall synthesis. It binds with high affinity to the D-alanyl-D-alanine terminus of the lipid II precursor in the bacterial cell wall. This binding physically blocks the transglycosylation and transpeptidation reactions required for cross-linking the peptidoglycan polymer, preventing elongation of the cell wall and leading to bacterial cell death.

Teicoplanin is bactericidal against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and Enterococcus faecalis. Its large molecular size prevents it from penetrating the outer membrane of Gram-negative organisms, giving it a selective spectrum limited to Gram-positive pathogens. Compared to vancomycin, teicoplanin has a significantly longer half-life of 70-100 hours, enabling once-daily dosing and making it more convenient for outpatient parenteral antimicrobial therapy.

Therapeutic Uses & Indications

Therapeutic Uses

Teicoplanin is indicated for the treatment of serious Gram-positive infections:

  • Methicillin-Resistant Staphylococcus aureus (MRSA) Infections: First-line treatment for MRSA bloodstream infections, pneumonia, and skin and soft tissue infections
  • Endocarditis: Effective against Gram-positive endocarditis, including Enterococcus faecalis
  • Bone and Joint Infections: Used in osteomyelitis and septic arthritis caused by susceptible organisms
  • Febrile Neutropenia: Part of empiric antibiotic therapy in immunocompromised patients
  • Surgical Prophylaxis: Used as prophylaxis in high-risk orthopedic and cardiac surgery patients

Why Manufacturers Choose Teicoplanin

Teicoplanin is strategically important for Indian pharmaceutical manufacturers as an alternative to vancomycin with a superior dosing profile and better tolerability. It was originally isolated from a soil sample in India (Nimodi Village, Indore), giving Indian manufacturers a unique advantage in raw material sourcing and production expertise. The lyophilized powder formulation at 200mg and 400mg strengths serves both hospital and export demand, particularly in European and Asian markets where teicoplanin is widely approved.

This makes Teicoplanin a high-value molecule for third party manufacturing in India, especially for WHO-GMP certified injectable facilities targeting regulated and semi-regulated markets.

Dosage Forms We Manufacture

Injection (Lyophilized Powder)
200 mg/vial · 400 mg/vial

Frequently Asked Questions

What is the minimum order quantity for Teicoplanin?
Minimum order quantity for Teicoplanin is Contact us for MOQ — varies by strength and batch size. Please contact us for bulk pricing and custom quantities.
What dosage forms of Teicoplanin can you manufacture?
We manufacture Teicoplanin as: Injection (Lyophilized Powder) (200 mg/vial, 400 mg/vial).
Are your manufacturing facilities WHO-GMP certified?
Yes. Celesta Healthcare works exclusively with WHO-GMP certified partner production facilities. All manufacturing batches are subject to strict quality control and documentation.
Can you manufacture Teicoplanin for export?
Yes. We provide export-ready Teicoplanin formulations structured across 25+ countries. We provide full export documentation including Certificate of Analysis (CoA), Certificate of Origin, and regulatory dossiers on request.
What grade standards do you follow for Teicoplanin?
We manufacture Teicoplanin to IP, BP, EP pharmacopoeial standards.
Third Party Manufacturing

Get Teicoplanin made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • Low MOQ, export ready
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+91 9689237122 · replies within hours

Our Manufacturing Capabilities

  • WHO-GMP Certified Partner Plants
  • 25+ years of pharma industry experience
  • PCD Franchise with monopoly rights
  • Export support across 25+ countries
  • Small batch to commercial scale
  • Custom formulation development

Packaging Options

Vial (lyophilized powder) with ampoule of water for injection. Available in single-dose vials, 1 vial per carton, 5 vials per carton. Packaging customized to client brand guidelines.

Start Manufacturing Teicoplanin Today

Celesta Healthcare provides WHO-GMP certified third-party manufacturing for Teicoplanin across all dosage forms. PCD franchise and export orders welcome.

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