100 Mg Carmustine For Injection USP
100 Mg Carmustine For Injection USP

100 Mg Carmustine For Injection USP

Price 3500 INR/ Vial

MOQ : 1 Vial

100 Mg Carmustine For Injection USP Specification

  • Dosage Form
  • Lyophilized Powder for Injection
  • Indication
  • Treatment of brain tumors, multiple myeloma, Hodgkins lymphoma, and non-Hodgkins lymphoma.
  • Salt Composition
  • Carmustine 100 mg
  • Feature
  • Single use vial; high purity; complies with USP standards
  • Ingredients
  • Carmustine USP, excipients
  • Application
  • Intravenous administration after reconstitution
  • Physical Color/Texture
  • Off-white to pale yellow lyophilized powder
  • Fermentation Smell
  • Odorless
  • Storage Instructions
  • Store below 25C, protected from light.
  • Shelf Life
  • 24 months
 
 

About 100 Mg Carmustine For Injection USP



Discover the distinguished 100 Mg Carmustine For Injection USP, presented in a single, sealed glass vial for uncompromising safety and pharmaceutical purity. Manufactured via aseptic lyophilization, this exclusive lyophilized powder is splendiferous for intravenous administration after reconstitution with sterile water. Designed for oncology and hospital professionals, it achieves sensational efficacy in treating brain tumors, multiple myeloma, and lymphomas. USP compliant, each batch guarantees analytical purity, and only prescription use ensures optimal control. Pick Yours-trusted by leading medical distributors, exporters, and suppliers across India.

A Sensational Solution for Oncology Treatment

100 Mg Carmustine For Injection USP is formulated for intravenous application on hospital surfaces, specifically for oncology and critical care settings. Its single-use vial and lyophilized powder dosage form offer competitive advantages, including high drug purity and guaranteed USP compliance. The distinguished manufacturing and purity standards assure clinicians and patients that each administration delivers precise, splendiferous formulation benefits during cancer therapies.


Sample Policy & Logistics: Expenditure, Freight, and Dispatch Details

100 Mg Carmustine For Injection USP samples are available for serious inquiries following a defined policy, ensuring cost expenditure, secure packaging, and timely dispatch. With robust supply ability, orders are efficiently dispatched via reliable freight networks. Each vial is carefully packaged and shipped below 25C, protected from light, guaranteeing integrity on arrival. Our commitment to prompt and secure delivery underscores our model as a trusted supplier and trader.


FAQ's of 100 Mg Carmustine For Injection USP:


Q: How is 100 Mg Carmustine For Injection USP reconstituted before use?

A: Reconstitute the lyophilized powder with sterile water for injection, following the instructions provided with the packaging. Once dissolved, the solution is ready for intravenous administration in a hospital setting.

Q: What is the main usage of Carmustine For Injection USP?

A: Carmustine For Injection USP is primarily used for the treatment of brain tumors, multiple myeloma, Hodgkin's lymphoma, and non-Hodgkin's lymphoma. It is intended for oncology professionals and hospital use only.

Q: When can I expect my order to be dispatched after placing it?

A: Orders for 100 Mg Carmustine For Injection USP are dispatched promptly after confirmation, following established sample policy and freight protocols to ensure timely delivery and maintain product integrity.

Q: Where should the vial be stored prior to use?

A: Store the sealed glass vial below 25C in a location protected from light to preserve pharmaceutical purity and efficacy, as specified in the storage instructions.

Q: What makes this product distinguished compared to competitors?

A: The distinguished Carmustine For Injection USP offers pharmaceutical purity validated by analytical certificate, manufactured using aseptic lyophilization, and complies fully with USP standards for reliable oncology applications.

Q: How does the high purity of this injection benefit patients?

A: Guaranteed high purity minimizes risks of impurities and maximizes clinical effectiveness, ensuring optimal therapeutic outcomes during cancer treatment, with every batch backed by analytical certification.

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