Tigecycline for Injection USP
Anti-Infectives & Antibiotics

Tigecycline for Injection USP

Pack Sizes Available

50mg single-dose vial, box of 1
50mg vial, tray with cover, export pack

Product Description

By the time a hospital reaches for Tigecycline, most of the easier options have already been tried and ruled out. This is the antibiotic that gets called in when multidrug-resistant organisms like MRSA, VRE, or ESBL-producing gram-negatives are in play, and standard first and second-line antibiotics are not going to cut it. As the first drug in the glycylcycline class, Tigecycline works differently from older tetracyclines, binding to the bacterial ribosome in a way that many resistance mechanisms simply have not evolved to counter yet. It is supplied as a 50mg lyophilized powder in a single-dose vial, reconstituted with saline or dextrose solution for intravenous infusion, and it covers two of the toughest categories in a hospital's infection control playbook: complicated skin and skin structure infections, and complicated intra-abdominal infections. Because it is so often the last well-supported option before physicians move to even more restricted antibiotics, availability matters enormously. A hospital that cannot source Tigecycline when a resistant infection shows up is in a genuinely difficult position. That is precisely why Sara Wellness treats this molecule with the seriousness it deserves. Over fifteen years of exporting critical care injectables from India, we have learned that last-line antibiotics cannot be treated like commodity products where a delayed shipment is a minor inconvenience. We work with GMP-certified manufacturing partners who understand the stakes, and our export team keeps stock levels and production schedules visible to key hospital and distributor accounts so nobody gets blindsided by a sudden gap in availability. We deal directly with buyers rather than routing orders through layers of brokers, which means when your pharmacy or procurement team has a question about a specific batch, reconstitution stability, or import documentation, you get an answer from someone who actually knows the product, not a generic support ticket. Our minimum order quantities are structured to work for hospital pharmacies stocking for occasional critical use as well as distributors building out a full infectious disease portfolio for a wider market. Every shipment travels with complete documentation, certificate of analysis, GMP compliance certification, and export paperwork prepared for your specific destination country's regulatory requirements. Given how tightly the API market for glycylcyclines is controlled by a small number of producers, pricing here moves more than buyers sometimes expect, and we quote current numbers rather than stale figures that will not hold up at order time. If a resistant infection protocol at your hospital or distribution network depends on reliable Tigecycline access, reach out with your country and expected volume, and our team will respond with real pricing and realistic lead times.

Technical Specifications

  • Active Ingredient: Tigecycline USP 50mg per vial
  • Dosage Form: Lyophilized powder for injection (SVP)
  • Drug Class: Glycylcycline antibiotic
  • Reconstitution: 5.3ml Sodium Chloride 0.9% or Dextrose 5% Injection, yields 10mg/ml
  • Route of Administration: Intravenous infusion
  • Storage Conditions: Store between 20-25 degrees Celsius, excursions 15-30 degrees Celsius permitted, protect from light
FAQ

Frequently asked questions

Contact Export TeamContact Export Team

Tigecycline is used to treat serious bacterial infections including complicated skin and skin structure infections and complicated intra-abdominal infections, particularly when multidrug-resistant organisms such as MRSA or ESBL-producing bacteria are involved.

As a glycylcycline antibiotic, Tigecycline binds reversibly to the bacterial ribosome, inhibiting protein synthesis and stopping bacterial growth, using a mechanism distinct from older tetracycline antibiotics which allows it to remain effective against many resistant strains.

Each 50mg vial is reconstituted with 5.3ml of 0.9% sodium chloride injection or 5% dextrose injection to achieve a concentration of 10mg per ml, then further diluted before administration by intravenous infusion, following the recommended dosing regimen of an initial 100mg loading dose followed by 50mg every 12 hours.

The standard adult regimen is an initial loading dose of 100mg, followed by a maintenance dose of 50mg administered intravenously every 12 hours, though the exact regimen should always be determined by the treating physician.

Prior to reconstitution, vials should be stored between 20 to 25 degrees Celsius, with excursions permitted between 15 to 30 degrees Celsius, and protected from light.

Yes, given the critical nature of this last-line antibiotic, we work closely with our manufacturing partners to maintain visibility on production schedules and keep key distributor and hospital accounts informed of stock status well in advance.

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