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Tocilizumab Injection
Tocilizumab Injection

Tocilizumab Injection

MOQ : 5000 Packs

Tocilizumab Injection Specification

  • Dosage Form
  • Injection
  • Salt Composition
  • Tocilizumab 80 mg/4 ml, 200 mg/10 ml, 400 mg/20 ml
  • Indication
  • Treatment of rheumatoid arthritis, systemic juvenile idiopathic arthritis, cytokine release syndrome (CRS), and COVID-19 related cytokine storm
  • Enzyme Types
  • Other
  • Feature
  • Ready-to-use vial, sterile, preservative-free
  • Ingredients
  • Other
  • Application
  • Other
  • Ph Level
  • 6.0-6.5 (approximate)
  • Temperature Needed For Fermentation
  • 2C to 8C storage, not applicable for fermentation
  • Physical Color/Texture
  • Clear to slightly opalescent, colorless to pale yellow solution
  • Fermentation Smell
  • Normal Smell
  • Enzymatic Activity
  • Not applicable; it is a monoclonal antibody
  • Storage Instructions
  • NORMAL TEMP
  • Shelf Life
  • 2 Years
  • Brand Name
  • Actemra (commonly known)
  • Route of Administration
  • Intravenous (IV) infusion or Subcutaneous injection
  • Vial Type
  • Single-use
  • Concentration
  • 20 mg/ml
  • Prescription Required
  • Yes
  • Compatibility
  • Compatible with 0.9% sodium chloride injection
  • Patient Population
  • Adults and pediatric patients (2 years and above)
  • Marketed By
  • Various pharmaceutical companies as per region
  • Packaging Size
  • 4 ml, 10 ml, 20 ml glass vials
  • Manufacturing Standard
  • cGMP certified
 

Tocilizumab Injection Trade Information

  • Minimum Order Quantity
  • 5000 Packs
  • FOB Port
  • Mumbai
  • Payment Terms
  • Cash in Advance (CID), Cash Advance (CA)
  • Supply Ability
  • Pack
  • Delivery Time
  • 7 Days
  • Sample Available
  • Yes
  • Sample Policy
  • Sample costs shipping and taxes has to be paid by the buyer
  • Packaging Details
  • STANDARD PACKNG
  • Main Export Market(s)
  • Australia, North America, South America, Eastern Europe, Western Europe, Middle East, Africa, Central America, Asia
  • Certifications
  • WHO GMP,ISO,FSSAI
 

About Tocilizumab Injection

Tocilizumab injection products (Actemra, Tyenne) are used to treat giant cell arteritis (a condition that causes swelling of blood vessels, especially in the scalp and head) in adults.


Versatile Dose Options and Administration

Tocilizumab Injection comes in 4 ml, 10 ml, and 20 ml vials, each suited to different dosing requirements. Whether administered intravenously or subcutaneously, it offers dosing flexibility for adults and pediatric patients (2 years and older). The solution is sterile, ready-to-use, and packaged in single-use glass vials to ensure quality and sterility every time.


Therapeutic Indications and Compatible Solutions

Primarily prescribed for rheumatoid arthritis, systemic juvenile idiopathic arthritis, cytokine release syndrome (CRS), and certain severe COVID-19 cases, Tocilizumab Injection is effective in modulating inflammatory responses. It is compatible with 0.9% sodium chloride injection, aiding in safe dilution for intravenous use as per medical advice.


Quality Manufacturing and Patient Safety

Manufactured under current Good Manufacturing Practice (cGMP) standards, Tocilizumab Injection ensures consistent potency and safety. Its clear solution, stable pH, and absence of preservatives minimize risk for sensitive individuals. The product's 2-year shelf life and specific storage instructions maintain its effectiveness until administration.

FAQ's of Tocilizumab Injection:


Q: How should Tocilizumab Injection be administered?

A: Tocilizumab Injection may be administered either as an intravenous infusion or as a subcutaneous injection, depending on the indication and patient requirements. Administration should only be performed by healthcare professionals in a clinical setting.

Q: What conditions is Tocilizumab Injection prescribed for?

A: Tocilizumab Injection is indicated for the treatment of rheumatoid arthritis, systemic juvenile idiopathic arthritis, cytokine release syndrome (CRS), and COVID-19 associated cytokine storm in adults and pediatric patients aged two years and above.

Q: When should Tocilizumab Injection be used during therapy?

A: Tocilizumab Injection is generally used when first-line treatments are insufficient or as directed for the approved indications by a healthcare provider. The timing and frequency depend on the disease being treated and the patient's response to therapy.

Q: Where should Tocilizumab Injection be stored?

A: The injection should be stored at a temperature between 2C and 8C (refrigerated), protected from light. Avoid freezing, and keep it in its original packaging until use to maintain sterility and efficacy.

Q: What is the benefit of single-use, preservative-free vials?

A: Single-use, preservative-free vials help reduce the risk of contamination and potential allergic reactions, ensuring each dose is sterile and safe for both adult and pediatric patients.

Q: How is Tocilizumab Injection prepared for IV administration?

A: For intravenous infusion, the required Tocilizumab dose is typically diluted in 0.9% sodium chloride injection. The preparation and administration should be carried out by qualified healthcare staff following manufacturer and prescribing information.

Q: What is the shelf life of Tocilizumab Injection and how can its potency be ensured?

A: Tocilizumab Injection maintains its potency for up to 2 years when stored correctly at 2C to 8C. Always check the expiration date before use and ensure the solution is clear to slightly opalescent without particulate matter.

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