About Tigecycline Injection USP 50mg
Specifications
| Manufacturer | Protech Telelinks |
| Composition | Tigecyclin |
| Prescription/Non prescription | Prescription |
| Form | Injection |
| Shelf life | Mfg-4/21, 3/23 |
| Batch No | LY072113A |
| Mfg Lic.No | N-MB/16/185 |
| Drug Name | Tigitech |
| Packaging Type | Vial |
| Strength | 50mg |
| Certification | WHO-GMP |
| Storage | Store Below 25 Degree C |
Precise Formulation for Critical InfectionsTigecycline Injection USP 50mg offers a reliable solution for treating severe bacterial infections in adults, such as complicated skin, intra-abdominal infections, and community-acquired pneumonia. Its formulation as a lyophilized powder maintains high potency and stability, making it suitable for healthcare settings.
Stringent Manufacturing and Quality StandardsManufactured in a WHO-GMP certified facility, each vial undergoes rigorous testing to ensure pharmaceutical-grade purity and compliance. The maintaining of pH between 4.5 and 5.5 after reconstitution guarantees optimal therapeutic effect and patient safety.
Convenient Handling and Storage RequirementsEach glass vial is intended for single-use and must be reconstituted with the specified diluent. Reconstituted solution should be used within 24 hours if stored refrigerated, must not be frozen, and any unused portion must be discarded to maintain safety and efficacy.
FAQ's of Tigecycline Injection USP 50mg:
Q: How should Tigecycline Injection USP 50mg be prepared for use?
A: Reconstitute the lyophilized powder in each vial with exactly 5.3 mL of either 0.9% Sodium Chloride or 5% Dextrose. Gently swirl the vial until the powder is completely dissolved and ensure the final pH is within 4.5-5.5 before administering intravenously.
Q: What medical conditions is Tigecycline Injection typically prescribed for?
A: Tigecycline Injection USP 50mg is indicated for the treatment of adults with complicated skin and intra-abdominal infections, as well as community-acquired bacterial pneumonia, as determined by a registered medical practitioner.
Q: When must the reconstituted solution be used, and how should it be stored?
A: After reconstitution, the solution must be used within 24 hours if kept refrigerated. It should not be frozen, and any leftover solution should be discarded to ensure patient safety.
Q: Where is Tigecycline Injection USP 50mg manufactured, and is it quality certified?
A: This product is made in a WHO-GMP certified facility, ensuring adherence to international standards for quality and safety in pharmaceutical production.
Q: What is the benefit of using Tigecycline Injection in adults?
A: Tigecycline's broad-spectrum activity provides an effective option against serious bacterial infections where other antibiotics might be less effective, particularly in adults with complex or resistant infections.
Q: What is the recommended dosage for Tigecycline Injection?
A: Dosage should always be determined and supervised by a registered medical practitioner. Strictly follow the doctor's instructions regarding dosage and administration route.