Ceftriaxone & Sulbactam for Injection 1.5gm
Anti-Infectives & Antibiotics

Ceftriaxone & Sulbactam for Injection 1.5gm

Pack Sizes Available

Single vial per box (export standard)
10 vials per box (hospital bulk pack)

Product Description

At the top of our ceftriaxone-sulbactam range sits this 1.5gm combination, built for serious infections where a physician needs both ceftriaxone's broad coverage and sulbactam's protection against beta-lactamase resistance, and needs it at a dose strong enough for severe hospital cases rather than routine outpatient treatment. Ceftriaxone & Sulbactam for Injection 1.5gm combines 1000mg of ceftriaxone with 500mg of sulbactam, supplied as a sterile powder for reconstitution and administered primarily by intravenous injection at this strength. It's used for severe respiratory infections, complicated intra-abdominal infections, septicemia, and other serious presentations where resistant organisms are a genuine concern and the treating physician wants the added assurance of a beta-lactamase inhibitor built into the formulation. Manufactured under GMP-compliant conditions, every batch undergoes testing not just for sterility and potency but for the correct ratio between the two active ingredients, since a combination antibiotic depends entirely on that balance being accurate. We don't treat this as a minor quality control checkbox given how much the formulation's effectiveness depends on it. Hospital pharmacies and tertiary care distributors sourcing this strength usually prioritize consistent batch quality and complete tender documentation above almost everything else. Fifteen years of exporting pharmaceutical products has put our regulatory and logistics teams through enough of these processes to know what buyers actually need before they have to ask twice. Pricing at this strength reflects the larger combined active content honestly, and we structure it to stay competitive on a comparative basis within this specific product category. Minimum order quantities scale with your operation, and every shipment includes a certificate of analysis alongside support for the registration paperwork your importing country requires. Storage before reconstitution stays simple: cool, dry, protected from light, no cold chain needed. If your hospital or distribution business needs this combination at its highest strength, reach out with your specific quantities and timeline, and expect a genuinely informed reply.

Technical Specifications

  • Drug Class: Third-generation cephalosporin with beta-lactamase inhibitor combination
  • Composition: Ceftriaxone Sodium equivalent to 1000mg Ceftriaxone + Sulbactam Sodium equivalent to 500mg Sulbactam per vial
  • Dosage Form: Sterile powder for reconstitution
  • Route of Administration: Intravenous (IV), or intramuscular (IM) where appropriate
  • Storage Conditions: Store below 25°C in a dry place, protected from light
  • Shelf Life: 24 months from date of manufacture, subject to storage conditions
FAQ

Frequently asked questions

Contact Export TeamContact Export Team

This combination is used for severe bacterial infections including complicated respiratory and intra-abdominal infections, septicemia, and other serious presentations where beta-lactamase producing resistant organisms are a clinical concern requiring both ceftriaxone and a beta-lactamase inhibitor.

It is typically given by intravenous injection or infusion, reconstituted with the diluent specified in the product insert, with dosing determined by the treating physician based on the severity of the infection and the patient's kidney function.

In infections where beta-lactamase producing resistant bacteria are suspected, plain ceftriaxone may be ineffective. The added sulbactam protects ceftriaxone from enzymatic breakdown, restoring its activity against these resistant organisms in more serious clinical scenarios.

Patients with known hypersensitivity to cephalosporins or penicillins should not receive this combination. Dose adjustment may be needed in patients with significant kidney impairment, and it should never be co-administered with calcium-containing solutions.

Institutional and government tender buyers receive a certificate of analysis for each batch, along with drug master file documentation and stability data, and support for the specific registration paperwork required by the importing country's regulatory authority.

The unreconstituted powder should be stored below 25°C in a dry environment away from direct light, and it does not require cold chain shipping. Vials are packed during export to guard against heat and moisture exposure, with shelf life confirmed at shipment.

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