Leuprorelin Acetate...

Leuprorelin Acetate Microspheres for Injection.

Leuprorelin Acetate Microspheres for Injection.

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0 Metric Ton

Negotiable

  • Min.Order :0 Metric Ton
  • Purity: 99%

Keywords

Formulation GnRHa

Quick Details

  • Appearance:white powder+water
  • Application:
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  • ProductionCapacity:|Metric Ton|Day
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Superiority:

 

 

 

The ONLY self-developed Long-term GnRH-a sustained release microsphere preparation in China

 

  • Material: Comply with BP standard with over 99% in purity.
  • Excipient: Self-researched and developed with better performance than exported PLGA.
  • Technology: High entrapment efficiency(96%) and drug-loading(8.7%) with mean particle size of 20
  • Quality: Strict quality management by complete control from material to final product.
  • Efficacy: Reliable in safety and performance proved by clinical verification and authorities.

 

 

 

Details:

Product Name
 Leuprorelin Acetate Microspheres for Injection.

Composition
 Main ingredients: copolymer of leuprorelin acetate and glycolide lactide 2575, gelatin, D-mannitol.

Indication
 1. Endometriosis
 2. Hysteromyoma reduce and/or improve hysteromyoma accompanied by hypermenorrhea, hypogastralgia, back pain and anaemia and etc.
 3. Premenopausal breast cancer with estrogen receptor positive.
 4. Prostate cancer.
 5. Central precocious puberty.

Dosage and Administration
 1. Endometriosis: subcutaneous injection. Generally, once every four weeks for adult with 3.75 mg each time. Initial dose should begin from 1-5 days of menstrual period.
 2. Hysteromyoma: subcutaneous injection. Generally, once every four weeks for adult with 1.88 mg each time. But patients with overweight or uterus increased significantly should be injected with 3.75 mg. Initial dose should begin from 1-5 days of menstrual period.
 3. Prostate cancer, premenopausal breast cancer with estrogen receptor positive: subcutaneous injection. Generally, once every four weeks for adult with 3.75 mg each time.
 4. Central precocious puberty: subcutaneous injection. Generally, once every four weeks with 30μg/kg each time, it can be increased to 90μg/kg according to the clinical symptoms of patients.
 Before injection, this product should be fully suspended with 2 ml solvent. Pay attention to no foam during the suspension.

How Supplied
 Injection vial, 3.75mg, 1 vial/box(1 vial+2 ml suspending agent).

Storage Condition
 Protect from light and keep tightly sealed in a cool place (store below 20 0C). 

Shelf Life
 18 months.

 

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