45 Mg Leuprolide Acetate Injection Suspension
45 Mg Leuprolide Acetate Injection Suspension

45 Mg Leuprolide Acetate Injection Suspension

Price 20000 INR/ Vial

MOQ : 1 Vial

45 Mg Leuprolide Acetate Injection Suspension Specification

  • Salt Composition
  • Leuprolide Acetate 45 mg
  • Indication
  • Advanced prostate cancer, endometriosis, uterine fibroids, and precocious puberty
  • Dosage Form
  • Injection Suspension
  • Feature
  • Long-acting depot formulation for sustained release
  • Ingredients
  • Leuprolide Acetate, sterile excipients
  • Application
  • Hormone therapy, gonadotropin-releasing hormone agonist treatment
  • Ph Level
  • Neutral (approximately 7)
  • Physical Color/Texture
  • White to off-white lyophilized powder in vial
  • Fermentation Smell
  • Odorless
  • Storage Instructions
  • Store in a refrigerator at 2-8°C
  • Shelf Life
  • 24 months
  • Disposal Instructions
  • Dispose after single use, follow local regulations for cytotoxic waste
  • Packaging Type
  • Single-use vial with prefilled diluent syringe
  • Reconstitution Instructions
  • Reconstitute with supplied diluent prior to use
  • Prescription Required
  • Yes
  • Regulatory Approval
  • Manufactured under GMP guidelines
  • Caution
  • For use under medical supervision only
  • Maximum Temperature Exposure
  • Do not freeze, avoid temperatures above 25°C
  • Sterility
  • Sterile preparation
  • Dose Strength
  • 45 mg per vial
  • Route of Administration
  • Subcutaneous or intramuscular injection
  • Latex Content
  • Latex-free packaging
  • Intended Patient Population
  • Adults
 
 

About 45 Mg Leuprolide Acetate Injection Suspension



Discover the renowned 45 Mg Leuprolide Acetate Injection Suspension, expertly formulated for inestimable efficacy against advanced prostate cancer, endometriosis, uterine fibroids, and precocious puberty. This top-tier hormone therapy features a long-acting depot formulation for sustained release, ensuring ineffable convenience with the lowest price guaranteed. Packaged in latex-free, single-use vials with a prefilled sterile diluent syringe, each dose guarantees pristine sterility and neutral pH. Pick yours for assured quality, manufactured under strict GMP guidelines. Prescription is required. Dispose safely after use and follow storage and reconstitution instructions.

Optimal Usage and Administration

45 Mg Leuprolide Acetate Injection Suspension is designed for adult patients, administered subcutaneously or intramuscularly for hormone therapy. The injection surface is typically the upper arm, thigh, or abdomen. Before use, reconstitute with the supplied diluent to achieve a homogeneous suspension. Its long-acting nature ensures sustained therapeutic effect, making it a trusted choice for managing complex hormonal disorders as prescribed by healthcare professionals.


Domestic Market and Logistics

The main domestic market for 45 Mg Leuprolide Acetate Injection Suspension covers major regions in India. Products are handled with care and handed over at designated FOB ports with reliable packaging standards. Sample policy allows for the provision of packaged samples to verified clients, supporting confidence and compliance within the domestic sphere. These protocols facilitate safe, prompt, and well-regulated distribution to authorized traders, suppliers, and exporters.


FAQ's of 45 Mg Leuprolide Acetate Injection Suspension:


Q: How should 45 Mg Leuprolide Acetate Injection Suspension be prepared for administration?

A: Before administration, reconstitute the lyophilized powder in the vial using the supplied prefilled diluent syringe to create a suspension. Ensure it is fully mixed before injecting subcutaneously or intramuscularly, as instructed by your healthcare provider.

Q: What are the main indications for using this injection suspension?

A: This product is primarily indicated for adults diagnosed with advanced prostate cancer, endometriosis, uterine fibroids, and precocious puberty. Always use under medical supervision and with a valid prescription.

Q: When should the reconstituted vial be used, and can it be reused?

A: The reconstituted vial should be used immediately after preparation and must be disposed of after single use. It is not designed for reuse; please follow local regulations for cytotoxic waste disposal.

Q: Where should the injection be administered on the body?

A: Administration is typically performed on subcutaneous sites such as the upper arm, thigh, or abdomen, or intramuscularly, depending on medical guidance.

Q: What are the recommended storage conditions for this injection suspension?

A: Store the vial in a refrigerator at 2-8C. Do not freeze or expose to temperatures above 25C to maintain efficacy and sterility.

Q: How does the long-acting depot formulation benefit patients?

A: The sustained-release depot formulation offers prolonged therapeutic effects, reducing the frequency of dosing and enhancing convenience for managing chronic hormonal conditions.

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