Aztreonam for Injection USP 1gm
Pack Sizes Available
Product Description
Technical Specifications
- Composition: Aztreonam USP equivalent to Anhydrous Aztreonam 1000mg, buffered with L-Arginine 780mg per vial
- Dosage Form: Sterile lyophilized powder for reconstitution, injection
- Route of Administration: Intramuscular (IM) or Intravenous (IV), as directed by physician
- Reconstitution Diluent: Sterile Water for Injection BP, approximately 10ml
- Appearance: White to off-white lyophilized powder or cake
- Storage Conditions: Store below 25°C, protect from light and moisture, keep in a cool dry place
- Shelf Life: 24 to 36 months from date of manufacture
- Packaging: Single vial per box; export cartons of 10 vials available
Aztreonam is a monobactam antibiotic used to treat infections caused by susceptible gram-negative aerobic bacteria, including urinary tract infections, lower respiratory tract infections, septicemia, skin and skin-structure infections, gynecological infections, and intra-abdominal infections. It is administered in hospital and clinical settings under medical supervision.
The lyophilized powder in each 1gm vial is reconstituted with approximately 10ml of Sterile Water for Injection BP. The vial is gently shaken until the powder dissolves completely into a clear solution. The reconstituted solution should be used promptly and any unused portion discarded, as per standard sterile injectable handling practice.
Aztreonam has a monocyclic beta-lactam structure that is chemically distinct from penicillins and most cephalosporins, which generally makes it a suitable option for patients with penicillin allergies. However, this determination must always be made by the treating physician based on the individual patient's allergy history.
Aztreonam for Injection USP 1gm typically carries a shelf life of 24 to 36 months from the date of manufacture, depending on the specific formulation batch. It should be stored below 25°C, protected from light and moisture, in a cool, dry place, and kept out of reach of children.
Yes, we supply Aztreonam for Injection USP 1gm in bulk export quantities with flexible MOQs suited to different market sizes. Private labeling and custom carton branding are available for distributors and importers who want the product supplied under their own brand name.
Each export order can be supplied with a full regulatory documentation package including Certificate of Analysis (COA), Certificate of Pharmaceutical Product (COPP), Free Sale Certificate (FSC), GMP certification, and stability data, formatted to meet the importing country's regulatory submission requirements.
Related Products
Explore more high-quality items from our Anti-Infectives & Antibiotics range.
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
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.
Ceftriaxone Injection 250mg
One injection a day instead of four is the kind of detail that sounds minor until you're the nurse actually administering it, or the patient on the receiving end. Ceftriaxone earned its place in outpatient and general ward treatment largely because of that once-daily dosing convenience, made possible by a half-life long enough to keep effective drug levels in the blood over a full 24 hours. Our 250mg strength is a third-generation cephalosporin supplied as a sterile powder for reconstitution, administered by intramuscular or intravenous injection. It covers a broad spectrum of gram-positive and gram-negative bacteria, making it a common choice for respiratory tract infections, urinary tract infections, and mild to moderate skin and soft tissue infections where a physician has determined ceftriaxone is the appropriate treatment. We manufacture this strength under GMP-compliant conditions and export it alongside our other ceftriaxone strengths, which range from 125mg for pediatric and single-dose use up through 1gm for more severe hospital cases. Buyers frequently order across this range rather than a single strength, and having one supplier handle the whole line keeps procurement, documentation, and batch traceability far simpler than sourcing from multiple vendors. Competitive pricing here isn't a slogan, it's a function of scale. Manufacturing a broadly used antibiotic strength in volume lets us pass real savings on to distributors, wholesalers, and pharmacy chains, while still maintaining the quality controls that a regulated pharmaceutical product demands. Minimum order quantities stay flexible enough for a first-time importer to place a manageable trial order and see how the relationship works before scaling up. For markets across Africa, Southeast Asia, the Middle East, the CIS region, and Latin America, where Sara Wellness has built export relationships over fifteen years, we handle the documentation side too, including certificates of analysis with every batch and support for whatever registration paperwork your local regulatory authority requires. Third-party pre-shipment inspection is available on request for buyers who want that extra check before goods leave India. Storage prior to reconstitution is straightforward: a cool, dry area away from direct light, no cold chain needed, which keeps freight simpler and cheaper regardless of destination. If you're stocking a pharmacy chain, supplying a hospital network, or fulfilling a government tender, reach out with your specific volume and timeline requirements, and expect a direct, informed reply rather than a generic catalogue response.