Ceftru-CV 100 Dry Syrup

Cefpodoxime 100 mg + Clavulanic Acid 62.5 mg Dry Syrup

Ceftru-CV 100 Dry Syrup — Cefpodoxime 100 mg + Clavulanic Acid 62.5 mg per 5 ml (Dry Syrup) from Trumac Healthcare PCD Pharma Franchise India

Composition Cefpodoxime 100 mg + Clavulanic Acid 62.5 mg per 5 ml (Dry Syrup)
Dosage Form Dry Syrup
Pack Type Bottle with Water
Pack Size 30 ml / 60 ml Bottle
MRP ₹ 1440
Therapy Paediatric + Antibiotic — Third-Gen Cephalosporin + Beta-Lactamase Inhibitor
Storage Dry powder below 30 °C. After reconstitution, refrigerate and use within 10 days.

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About Ceftru-CV 100 Dry Syrup

Ceftru-CV 100 Dry Syrup is the higher-strength paediatric combination of Cefpodoxime 100 mg with Clavulanic Acid 62.5 mg per 5 ml. Used in older children and adolescents requiring higher cefpodoxime doses with beta-lactamase coverage.

The 100/62.5 mg ratio maintains the standard 1.6:1 cefpodoxime:clavulanate ratio, providing effective enzyme inhibition for the higher antibiotic dose. Suited to complicated paediatric otitis media, sinusitis, pneumonia and skin infections.

Ceftru-CV 100 Dry Syrup is manufactured by Trumac Healthcare under WHO-GMP conditions. Available for monopoly-based PCD pharma franchise and third-party manufacturing.

Indications

  • Complicated paediatric otitis media
  • Severe paediatric sinusitis
  • Community-acquired pneumonia in older children
  • Paediatric skin and soft-tissue infections with beta-lactamase suspicion

Mechanism of Action

Cefpodoxime Proxetil is an oral third-generation cephalosporin prodrug that is hydrolysed in intestinal mucosa to active cefpodoxime. It binds penicillin-binding proteins, inhibiting peptidoglycan cross-linking. Broad spectrum covering gram-negative (H. influenzae, M. catarrhalis, E. coli, Klebsiella) and selected gram-positive (streptococci, MSSA) organisms — including many beta-lactamase-producing strains. Clavulanate inhibits beta-lactamases.

Dosage & Administration

Children > 5 years: 10 mg/kg/day of cefpodoxime in two divided doses for 7–10 days. Reconstitute with supplied water; refrigerate after reconstitution.

Side Effects

Diarrhoea, nausea, vomiting, mild rash, headache. Rare: pseudomembranous colitis, anaphylaxis, severe skin reactions. Cross-reactivity with penicillin allergy (~5–10%). Increased GI upset due to clavulanate.

Contraindications & Precautions

Hypersensitivity to cephalosporins. Severe penicillin allergy. Caution in renal impairment (dose adjustment). Caution in GI disease. History of cholestatic jaundice with clavulanate.

Storage

Dry powder below 30 °C. After reconstitution, refrigerate and use within 10 days.

PCD Pharma Franchise & Third-Party Manufacturing
Ceftru-CV 100 Dry Syrup is available for monopoly-based PCD pharma franchise across India and for third-party manufacturing under your brand. WHO-GMP certified, with full visual-aid and promotional support. Become a Trumac franchise partner →

Frequently Asked Questions

What is Ceftru-CV 100 Dry Syrup used for?

Ceftru-CV 100 Dry Syrup contains Cefpodoxime 100 mg + Clavulanic Acid dry syrup and is used for bacterial infections — UTI, ENT, respiratory tract, skin/soft-tissue infections in the appropriate age group.

How long is the course?

Typical course is 5–10 days; longer in complicated infections. Always complete the prescribed course.

Is Ceftru-CV 100 Dry Syrup available for PCD pharma franchise?

Yes, Trumac Healthcare offers Ceftru-CV 100 Dry Syrup on monopoly-based PCD pharma franchise and for third-party manufacturing.

How should Ceftru-CV 100 Dry Syrup be stored?

Store below 30 °C in a dry place, protected from light and moisture.

Is Ceftru-CV 100 Dry Syrup WHO-GMP certified?

Yes, manufactured in WHO-GMP and DCGI-compliant facilities.

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B2B Disclaimer: This page is part of a Business-to-Business (B2B) pharmaceutical catalog intended for distributors, PCD franchise partners and healthcare professionals. Information provided is for commercial and educational reference only. Not for consumer sale. Patients must not self-medicate; please consult a qualified medical practitioner. All trade inquiries are subject to valid Drug License and GST documentation.