Cefoperazone Injection 500mg
Anti-Infectives & Antibiotics

Cefoperazone Injection 500mg

Pack Sizes Available

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

Product Description

A cephalosporin that leaves the body mostly through bile rather than the kidneys sounds like a small pharmacological footnote until you're treating a patient whose renal function is already compromised. That's the practical reason cefoperazone still gets prescribed decades after its introduction, and the 500mg strength is the one that fits a wide range of general adult dosing scenarios without stepping up to the full 1gm vial. Cefoperazone Injection 500mg is a third-generation cephalosporin, supplied as a sterile powder for reconstitution ahead of intramuscular or intravenous administration. Clinicians reach for it in respiratory tract infections, urinary and genital tract infections, skin and soft tissue infections, and biliary tract infections, given its favorable excretion pathway and broad activity against gram-negative and gram-positive organisms. We manufacture this product under GMP-compliant conditions, with each batch tested for sterility and potency before packaging, and a certificate of analysis accompanies every shipment as a matter of standard practice rather than a special request. For distributors and hospital pharmacies, that kind of consistency is what actually builds a long-term supply relationship, more so than any single marketing claim about the product itself. Export pricing stays competitive because we manufacture at real scale rather than treating this as a niche side offering, and that scale gets passed along to buyers across Africa, Southeast Asia, the CIS region, and Latin America, where we've built export relationships over fifteen years. Minimum order quantities flex to accommodate a smaller distributor's first trial order just as readily as a larger hospital network's standing supply contract. Registration paperwork and drug master file documentation are prepared according to the specific requirements of your importing country, and we're glad to arrange third-party pre-shipment inspection where your local regulations call for it. None of this replaces the underlying quality of the product, but it does mean the paperwork won't be the reason a shipment gets held up. Storage before reconstitution needs only a cool, dry environment away from direct light, with no cold chain shipping required, keeping logistics manageable across different climates. If you're stocking a hospital pharmacy or distribution business with cefoperazone, reach out with your specific volume and timeline requirements and expect a direct, informed reply.

Technical Specifications

  • Drug Class: Third-generation cephalosporin antibiotic
  • Composition: Cefoperazone Sodium IP equivalent to 500mg Cefoperazone per vial
  • Dosage Form: Sterile powder for reconstitution
  • Route of Administration: Intramuscular (IM) or Intravenous (IV)
  • 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

Cefoperazone Injection 500mg is used to treat respiratory tract infections, urinary and genital tract infections, skin and soft tissue infections, and biliary tract infections caused by susceptible bacteria, as determined by the treating physician.

Because cefoperazone is largely eliminated through the biliary system rather than the kidneys, it is sometimes considered a reasonable option for patients with renal impairment, though the treating physician should still assess overall kidney function and adjust monitoring as needed.

The sterile powder is reconstituted with the diluent specified in the product insert and given by intramuscular injection or by intravenous injection or infusion, with the exact dose and frequency determined by the treating physician based on the infection being treated.

Common side effects include diarrhea, nausea, and injection site reactions. Cefoperazone can also affect vitamin K-dependent clotting factors in some patients, so it should be used cautiously in those with bleeding disorders or on anticoagulant therapy.

Yes, alcohol should be avoided during treatment with cefoperazone and for a few days afterward, since a disulfiram-like reaction involving flushing, nausea, and a rapid heartbeat has been reported when certain cephalosporins are combined with alcohol.

The unreconstituted powder should be stored in a cool, dry place, generally below 25°C, protected from light, and does not require cold chain shipping. Buyers should confirm remaining shelf life at the time of shipment to match their expected usage timeline.

You might also like

Related Products

Explore more high-quality items from our Anti-Infectives & Antibiotics range.

Aztreonam for Injection USP 1gm
Anti-Infectives & Antibiotics

Aztreonam for Injection USP 1gm

Bacterial infections don't wait for perfect conditions, and neither should a hospital's antibiotic stock. Aztreonam occupies a specific and useful place in that stock: a monobactam, structurally distinct from penicillins and cephalosporins, built to target gram-negative aerobic organisms with minimal cross-reactivity concerns for patients with beta-lactam allergies. That distinction matters more to procurement teams than it might first appear, because it means this molecule fills a gap other antibiotics in a formulary simply cannot. Each vial of this 1gm formulation contains sterile Aztreonam USP, buffered with L-Arginine, supplied as a lyophilized powder ready for reconstitution with Sterile Water for Injection. The powder dissolves cleanly, reconstitutes without excessive foaming, and yields a solution suited for both intramuscular and intravenous administration depending on clinical protocol. Hospitals value predictability in a product like this, and predictability is exactly what a well-controlled lyophilization process delivers, batch after batch. We manufacture and export this product under WHO-GMP compliant conditions, with full documentation available for buyers who need it: COA, COPP, Free Sale Certificate, stability data, and regulatory dossiers formatted for the destination market's requirements. Fifteen years in the export business has taught us that paperwork delays cost more than the product itself, so we keep documentation ready before a buyer even asks. Packaging is built around what actually moves through customs and hospital pharmacies without friction. Single vials, ten-vial export cartons, cold-chain-appropriate secondary packaging where required, and labeling that can be customized to a country's language and regulatory format. Private labeling is available for distributors who want their own brand on the box, a request we handle often enough that it barely counts as a special case anymore. Pricing works on volume, and we structure it that way deliberately. A first-time importer testing the market with a modest order gets a fair quote. A returning distributor placing a container-load order gets a better one. MOQs flex based on what a buyer's market actually needs, not on some rigid internal policy that ignores the reality of different countries having very different demand curves. Somebody in West Africa and somebody in Eastern Europe are not buying antibiotics the same way, and we don't pretend they are. Communication stays direct. One point of contact, no ticket queues, no three-week wait for a simple stock update. If a shipment date shifts, you hear about it before you have to ask. If a regulatory document needs a signature or a stamp, we chase it down rather than leaving the buyer to track it themselves. Lead times are quoted honestly, which sounds like a low bar until you've dealt with suppliers who quote optimistically and deliver whenever. Cold chain logistics, when required, are handled through partners experienced specifically in pharmaceutical shipping, not general freight forwarders learning temperature control on the job. For importers building a critical care or hospital antibiotic line, this is a product worth having a reliable source for, and reliability is the entire pitch here.

Cloxacillin Injection 1.0gm
Anti-Infectives & Antibiotics

Cloxacillin Injection 1.0gm

Severe staphylococcal infections don't leave much room for undertreatment, which is exactly why the 1 gram vial exists alongside the 250mg and 500mg strengths in our cloxacillin range. When a physician is managing endocarditis, deep-seated osteomyelitis, or septicemia caused by beta-lactamase producing staphylococci, the higher single-vial dose reduces the number of reconstitutions and injections a critically ill patient needs to go through in a day. Cloxacillin Injection 1.0gm is supplied as a sterile powder containing cloxacillin sodium equivalent to 1 gram of cloxacillin, manufactured under GMP conditions and intended for intramuscular or, more commonly at this strength, intravenous administration. Being a penicillinase-resistant penicillin, it remains active against strains that would otherwise render ordinary penicillin useless, which is the entire reason this drug class still holds a place in hospital antibiotic formularies decades after its introduction. Buyers sourcing the 1gm strength are usually hospital pharmacies, tertiary care distributors, or government procurement programs managing ICU-level antibiotic stock, and their concerns tend to run a little different from a retail pharmacy chain. Consistency across batches matters enormously when a hospital's protocol depends on predictable dosing, and documentation needs to be airtight for tender submissions. We've supported exactly this kind of buyer for fifteen years, and our regulatory team is used to preparing the drug master files, CoAs, and stability data that these processes require. Pricing at this strength is naturally higher per vial than the 250mg or 500mg versions, but we structure our export pricing to stay competitive on a per-milligram basis, since that's really what a buyer comparing suppliers is calculating anyway. Minimum order quantities flex with the size of your operation. A first-time distributor testing our product against a competitor's gets the same attentive handling as a returning government buyer placing a large tender order. Logistics for this product are relatively simple since it doesn't require cold chain shipping, just protection from heat, moisture, and direct light during transit. We package accordingly, and every shipment travels with a certificate of analysis. Third-party inspection can be arranged for markets where that's part of the import process, and our team handles the paperwork side of registration support for countries across Africa, the CIS region, Southeast Asia, and Latin America where we already have an established export history. Given that this strength is often ordered for hospital or institutional use, we're happy to walk through batch traceability, cold storage alternatives if your climate demands it, or private labeling options if you're building your own branded line. Reach out directly with your requirements and expect a real, specific answer rather than a generic brochure reply.

Cloxacillin Injection 500mg
Anti-Infectives & Antibiotics

Cloxacillin Injection 500mg

Ask any hospital pharmacist which antibiotic vial they reorder most often for staph coverage and Cloxacillin 500mg tends to come up fast. It sits at the strength most adults actually get prescribed, which makes it the workhorse version of the three we manufacture. The 250mg and 1gm vials matter too, but 500mg is the one that keeps formularies stocked week after week. This is cloxacillin sodium, a penicillinase-resistant penicillin, supplied as a sterile powder for reconstitution ahead of intramuscular or intravenous use. It targets infections caused by beta-lactamase producing staphylococci, the strains that render ordinary penicillin useless. Clinicians reach for it in skin and soft tissue infections, respiratory infections, and, at physician discretion, more serious conditions like bone or bloodstream infections where staphylococcal resistance is a known concern. We manufacture it under GMP-compliant conditions at our partner facilities, and every batch is tested for potency and sterility before it leaves for packaging. None of that matters much to a buyer, though, until it shows up as a certificate of analysis attached to your shipment, which is exactly how we handle it. If your import authority wants third-party verification on top of that, we arrange it without turning it into a negotiation. Sourcing pharmaceutical injectables from an unfamiliar country can feel risky the first time, especially for buyers who have been burned before by suppliers who overpromised on lead times or underdelivered on documentation. We've spent fifteen years building relationships with distributors, wholesalers, and hospital procurement teams across Africa, the Middle East, Southeast Asia, and Latin America precisely because those relationships depend on doing the boring parts right: correct labeling, correct paperwork, and shipments that arrive when we said they would. Minimum order quantities are flexible rather than fixed at some arbitrary threshold that only suits large-scale buyers. A smaller distributor testing the market gets treated the same as a returning client with a standing order. Pricing reflects volume, obviously, but it's never inflated for the sake of it. Storage before use is uncomplicated. Keep the sealed vials cool, dry, and out of direct sunlight, and the powder holds its potency comfortably through the labeled shelf life. Once reconstituted, though, timing matters, and hospital staff should follow the product insert closely regarding usable duration after mixing. Whether you're placing a first trial order or restocking a running contract, reach out with your specific requirements, whether that's batch documentation, freight terms, or private labeling for your own market. You'll get a direct answer from someone who actually knows this product, not a form response.