440 Mg Trastuzumab Injection
440 Mg Trastuzumab Injection

440 Mg Trastuzumab Injection

Price 20000 INR/ Box

MOQ : 1 Box

440 Mg Trastuzumab Injection Specification

  • Salt Composition
  • Trastuzumab 440 mg
  • Dosage Form
  • Lyophilized Powder for Injection
  • Indication
  • Breast cancer, Gastric cancer, HER2-positive cancers
  • Feature
  • Monoclonal antibody therapy for HER2-positive cancers
  • Ingredients
  • Trastuzumab, excipients
  • Application
  • Intravenous use only
  • Ph Level
  • 6.0 ± 0.2
  • Physical Color/Texture
  • White to pale yellow powder
  • Fermentation Smell
  • Odorless
  • Storage Instructions
  • Store at 2°C to 8°C. Do not freeze.
  • Shelf Life
  • 24 Months
  • Type of Packaging
  • Single-use glass vial
  • Therapeutic Class
  • Antineoplastic (targeted therapy)
  • Drug Type
  • Biosimilar/Reference Biologic
  • Reconstitution Instructions
  • Reconstitute with provided sterile water for injection
  • Dosage Frequency
  • As directed by oncologist
  • Warning
  • For hospital use only; cardiac monitoring required
  • Prescription/OTC Status
  • Prescription only
  • Molecular Formula
  • C6470H10012N1726O2013S42
  • Regulatory Approval
  • WHO-GMP, DCGI approved
  • Box Contents
  • Powder vial, solvent vial, leaflet
  • Strength
  • 440 mg per vial
  • Contraindication
  • Hypersensitivity to trastuzumab or any excipients
  • Marketed By
  • According to label (varies)
  • Pack Size
  • 1 Vial (440 mg) with 1 vial of 20 ml sterile water for injection
  • Solubility After Reconstitution
  • Clear to opalescent, colorless to pale yellow solution
  • Inactive Ingredients
  • L-histidine, polysorbate 20, sucrose
  • Patient Age Group
  • Adult
  • Route of Administration
  • Intravenous infusion
 
 

About 440 Mg Trastuzumab Injection



Order the trending 440 mg Trastuzumab Injection-a matchless monoclonal antibody therapy decorated with WHO-GMP and DCGI approvals. Each package includes a single-use glass vial containing white to pale yellow lyophilized powder and a vial of 20 ml sterile water for injection. Designed for enlightened hospital use, this product provides targeted therapy for HER2-positive breast and gastric cancers. Reconstitute as instructed and administer via intravenous infusion, ensuring cardiac monitoring. Strictly prescription-only, storing at 2C to 8C helps preserve stability. With markdown pricing available for qualified distributors, this biosimilar/reference biologic underlines therapeutic excellence.

Applications and Usage of 440 Mg Trastuzumab Injection

The 440 mg Trastuzumab Injection is primarily utilized in treating HER2-positive cancers, such as breast and gastric cancer, in adults. Decorated for its efficacy as an antineoplastic agent, it is prescribed as a targeted therapy and administered intravenously. This product is also suited for combination with chemotherapy as directed by an oncologist. Its matchless effectiveness makes it a top choice for oncological regimes requiring biosimilar monoclonal antibody use.


Payment Terms, Dispatch, and Market Coverage

We offer flexible payment terms with options to place orders at a competitive list price for single or bulk requirements. Products are dispatched promptly through reliable logistics partners to ensure delivery across all major domestic markets in India. Samples can be requested for regulated hospital use, providing a practical opportunity for evaluation before large-scale orders. Our logistics solutions are streamlined for hassle-free procurement, allowing distributors, exporters, and traders to benefit efficiently.


FAQ's of 440 Mg Trastuzumab Injection:


Q: How should the 440 mg Trastuzumab Injection be reconstituted before administration?

A: The vial must be reconstituted with the supplied 20 ml sterile water for injection as per the leaflet instructions. After proper mixing, the solution should be clear to opalescent before intravenous infusion.

Q: What are the main benefits of using 440 mg Trastuzumab Injection in cancer therapy?

A: Trastuzumab offers targeted therapy for HER2-positive breast and gastric cancers, providing matchless efficacy in slowing tumor growth and improving patient outcomes compared to traditional treatments.

Q: When is cardiac monitoring required with Trastuzumab administration?

A: Cardiac monitoring is required during and after infusion due to the risk of adverse cardiac events, especially in patients with previous heart conditions or concurrent chemotherapy use.

Q: Where is the 440 mg Trastuzumab Injection typically administered?

A: This medication is administered in a hospital or clinical setting, under the supervision of trained oncology healthcare professionals, and is strictly for prescription use only.

Q: What precautions must be taken regarding storage of this product?

A: The injection should be stored between 2C to 8C and must never be frozen. Adhering to these storage instructions maintains its stability and efficacy.

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