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Dacarbazine Injection

Dacarbazine Injection
Dacarbazine Injection

Dacarbazine Injection Specification

  • Indication
  • Used in the treatment of Hodgkins lymphoma, malignant melanoma, and soft tissue sarcoma
  • Dosage Form
  • Injection
  • Salt Composition
  • Dacarbazine (Lyophilized) 200 mg/vial
  • Enzyme Types
  • Not applicable (synthetic cytotoxic agent)
  • Feature
  • Sterile, single-dose, preservative-free
  • Ingredients
  • Application
  • Intravenous use
  • Ph Level
  • Approximately 3 - 4 after reconstitution
  • Physical Color/Texture
  • White to off-white lyophilized powder
  • Fermentation Smell
  • Odorless or faint chemical odor
  • Storage Instructions
  • Store below 25C, protect from light
  • Shelf Life
  • 2 years
  • Disposal Instructions
  • Dispose of unused product and waste materials in accordance with local requirements
  • USP/Pharmacopoeial Reference
  • USP/Ph.Eur. standards
  • Hazard Class
  • Cytotoxic - handle with care
  • Pack Size
  • Single vial (200 mg)
  • Administration Route
  • Intravenous infusion only
  • Compatibility
  • Compatible with 0.9% Sodium Chloride after reconstitution
  • Packaging Type
  • Glass vial, sealed with rubber stopper and aluminum cap
  • Contraindication
  • Hypersensitivity to dacarbazine or any excipients
  • Reconstitution Solution
  • Sterile Water for Injection
  • Regulatory Status
  • Prescription only (Rx)
 
 

About Dacarbazine Injection

 Dacarbazine Injection:-

Brand Name: Dacarex
Contents: Dacarbazine
International Brands:
  • DTIC-Dome
Manufacturer Alkem (Cytomed)
Strength Available: 100mg / 200mg / 500mg
Packing: Price per Vial

 

 



Efficient Management of Cancers

Dacarbazine Injection is widely used in oncology for its effectiveness against specific cancers such as Hodgkins lymphoma, malignant melanoma, and soft tissue sarcoma. Its cytotoxic action interferes with cancer cell growth and proliferation, offering promising outcomes when administered according to prescribed guidelines. The products compliance with international standards ensures reliability and safety in clinical settings.


Strict Safety and Handling Protocols

Given its classification as a cytotoxic agent, Dacarbazine Injection must be handled with caution. Healthcare professionals follow strict protocols for preparation and disposal to minimize exposure risks. The vial is single-use and preservative-free, enhancing safety and maintaining sterility during administration. Proper disposal of unused products and materials is required to conform with local regulatory policies.


Storage, Dosage, and Shelf Life Information

Dacarbazine Injection is stable for up to two years when stored below 25C and protected from light. The vial contains a white to off-white lyophilized powder to be reconstituted immediately before infusion. Strict adherence to dosage, administration, and reconstitution guidelines is vital for patient safety and effectiveness.

FAQs of Dacarbazine Injection:


Q: How should Dacarbazine Injection be prepared and administered?

A: Dacarbazine Injection must be reconstituted with Sterile Water for Injection and may be further diluted with 0.9% Sodium Chloride for intravenous infusion. The solution should be prepared aseptically and infused as directed by a healthcare professional.

Q: What are the main benefits of using Dacarbazine Injection in cancer treatment?

A: Dacarbazine Injection is highly effective in treating Hodgkins lymphoma, malignant melanoma, and soft tissue sarcoma. Its mechanism of action targets and inhibits cancer cell growth, contributing to improved patient outcomes under appropriate medical supervision.

Q: When is Dacarbazine Injection contraindicated?

A: This product is contraindicated in patients with known hypersensitivity to dacarbazine or any of its excipients. It should not be used if patients demonstrate allergic reactions to any component of the formulation.

Q: Where should Dacarbazine Injection be stored to maintain quality and safety?

A: Store the vials below 25C and protect them from light. Proper storage conditions are essential to ensure the products sterility and effectiveness until its 2-year shelf life expires.

Q: What are the disposal requirements for Dacarbazine Injection and associated materials?

A: All unused solution, vials, and medical waste must be disposed of in accordance with local regulatory guidelines for cytotoxic agents to prevent environmental contamination and accidental exposure.

Q: How is Dacarbazine Injection supplied, and who can access this medication?

A: This medication is available as a single vial containing 200 mg of lyophilized dacarbazine, distributed to licensed healthcare providers, hospitals, and authorized dealers or wholesalers. It is only available via prescription in India.

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