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JAYPEE PHARMACARE

GST : 24BAYPS0913F1ZI

100mg Xpreza Azacitidine Injection
100mg Xpreza Azacitidine Injection

100mg Xpreza Azacitidine Injection

Price 4250.0 INR/ Piece

MOQ : 10 Pieces

100mg Xpreza Azacitidine Injection Specification

  • Salt Composition
  • Azacitidine 100mg
  • Life Span
  • 2 years (from date of manufacture)
  • Brand Name
  • Xpreza
  • Pacakaging (Quantity Per Box)
  • 1 vial per box
  • Packaging Type
  • Vial
  • Dosage Form
  • Powder for injection
  • Indication
  • Treatment of myelodysplastic syndromes
  • Origin of Medicine
  • India
  • Drug Type
  • Ingredients
  • Azacitidine
  • Physical Form
  • Injection
  • Function
  • Recommended For
  • Adults with myelodysplastic syndromes
  • Dosage
  • 100 mg per vial
  • Dosage Guidelines
  • As directed by physician
  • Suitable For
  • Adults
  • Storage Instructions
  • Store below 25C, protect from light
  • Shelf Life After Reconstitution
  • Use immediately or within 1 hour at 2C - 8C
  • Marketed By
  • Natco Pharma Limited
  • Prescription/Non-Prescription
  • Prescription
  • Route of Administration
  • Subcutaneous or intravenous injection
  • Therapeutic Class
  • Antineoplastic Agent
  • Reconstitution Solvent
  • Sterile water for injection
  • Appearance
  • White to off-white lyophilized powder
  • Regulatory Approval
  • WHO-GMP Certified, DCGI Approved
 
 

About 100mg Xpreza Azacitidine Injection

Strength 100 mg
Form Injection
Brand Xpreza
Manufacturer Natco
Packaging Type Vial
Prescription/Non prescription Prescription
Packaging Size 100 ml

Xpreza Injection is used to treat myelodysplastic syndrome, a group of conditions in which the bone marrow produces blood cells that are abnormal in structure and function, and does not produce enough healthy blood cells.

Reliable Therapy for Myelodysplastic Syndromes

Xpreza Azacitidine Injection delivers targeted and clinically-proven chemotherapy for adults diagnosed with myelodysplastic syndromes. Its formulation ensures effective management of abnormal blood cell production, supporting improved patient outcomes in this complex condition.


Quality-Assured Manufacturing

Manufactured and marketed in India by Natco Pharma Limited, Xpreza is both WHO-GMP certified and DCGI approved. This guarantees stringent quality standards, offering peace of mind for healthcare providers and patients alike.


Simple Preparation and Administration

Each vial of Xpreza must be reconstituted with sterile water for injection, as provided. The freshly prepared solution should be used immediately or stored for up to one hour at 2C-8C, delivering flexibility and safety during administration, either subcutaneously or intravenously.

FAQ's of 100mg Xpreza Azacitidine Injection:


Q: How should Xpreza Azacitidine Injection be reconstituted and administered?

A: Xpreza must be reconstituted with the supplied sterile water for injection. The solution should be prepared freshly before use and administered either subcutaneously or intravenously as directed by a physician.

Q: What is the recommended dosage for Xpreza Azacitidine Injection?

A: The typical dosage is 100mg per vial. The exact dosage regimen and duration depend on your specific condition and will be determined by your healthcare provider.

Q: When should the reconstituted solution be used and how should it be stored?

A: Once reconstituted, the Xpreza solution should be used immediately. If needed, it can be stored at 2C-8C and must be used within one hour to ensure efficacy and safety.

Q: Where should Xpreza Azacitidine Injection be stored before use?

A: Keep the unopened vials stored below 25C and protect them from light. Follow all storage guidelines to preserve the quality and effectiveness of the medication.

Q: What are the benefits of using Xpreza for myelodysplastic syndromes?

A: Xpreza helps manage abnormal blood cell production in adults with myelodysplastic syndromes, potentially delaying disease progression and improving quality of life.

Q: Who can be prescribed Xpreza Azacitidine Injection?

A: Xpreza is indicated for adult patients diagnosed with myelodysplastic syndromes and is available only by prescription. Suitability and use must be assessed and supervised by a healthcare professional.

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