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Ceftazidime and Avibactam Injection

This formulation consists of:

  • Active Ingredients: Ceftazidime (2000 mg) and Avibactam (500 mg)

  • Pharmaceutical Grade Excipients: Sterile, pyrogen-free diluent (WFI – Water for Injection)

Benefits:

  • Provides broad-spectrum antibacterial activity against multidrug-resistant Gram-negative bacteria

  • Effective in treating complicated intra-abdominal, urinary tract, and respiratory infections

  • Combines a third-generation cephalosporin with a β-lactamase inhibitor for enhanced efficacy

  • Restores the activity of ceftazidime against resistant bacterial strains

  • Demonstrates excellent safety and clinical success rates

Available Variations in formulations:

We offer Ceftazidime and Avibactam Injection in the following strengths:
  • 2.5 gm (Ceftazidime 2 gm + Avibactam 0.5 gm)

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Product Details

Ceftazidime and Avibactam Injection 2.5 gm is a sterile, parenteral antibacterial combination used for the treatment of severe infections caused by Gram-negative bacteria, including resistant strains producing extended-spectrum β-lactamases (ESBLs) and carbapenemases.

Ceftazidime, a third-generation cephalosporin, inhibits bacterial cell wall synthesis, while Avibactam, a non-β-lactam β-lactamase inhibitor, protects Ceftazidime from enzymatic degradation. Together, they provide potent and broad antibacterial coverage.

This combination is indicated for hospital-acquired infections, intra-abdominal infections, and urinary tract infections in adult and pediatric patients. The formulation ensures consistent plasma levels and reliable clinical efficacy when administered intravenously.

Indications
  • Complicated intra-abdominal infections (cIAI)

  • Complicated urinary tract infections (cUTI), including pyelonephritis

  • Hospital-acquired and ventilator-associated bacterial pneumonia (HABP/VABP)

  • Infections caused by multidrug-resistant Enterobacteriaceae and Pseudomonas aeruginosa

Dosage
  • Adults: 2.5 gm (Ceftazidime 2 gm + Avibactam 0.5 gm) every 8 hours, administered by intravenous infusion over 2 hours

  • Dosage adjustment is required for patients with renal impairment

Use under the supervision of a qualified healthcare professional only

Uses

N/A

Side Effects

N/A

Packaging Volume

Vial Pack + WFI

Minimum Order Quantity

15,000 Units

Delivery Time

45–60 Business Days

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Corporate Office
Plot No. :46 First Floor, Industrial Area Phase-2, Chandigarh-160002, India.

Manufacturing Unit
Village Kondi, Post Thana, District Solan, Baddi 173205 Himachal Pradesh, India.

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