Eribulin Mesylate Injection

Eribulin Mesylate Injection
Business Type Exporter, Supplier
API Form Liquid
Dosage As per Doctor's Prescription
Type Intravenous Administration
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Preferred Buyer From

Location Worldwide

Product Details

Storage
Cool and Dry Place
Best Before
36 Months from Manufacturing

On January 28, 2016, the U. S. Food and Drug Administration approved eribulin (HALAVEN injection, Eisai Co., Ltd.) for the treatment of patients with unresectable or metastatic liposarcoma who have received a prior anthracycline-containing regimen.


 


HALAVEN is a microtubule inhibitor indicated for the treatment of patients with metastatic breast cancer who have previously received at least two chemotherapeutic regimens for the treatment of metastatic disease. Prior therapy should have included an anthracycline and a taxane in either the adjuvant or metastatic setting .

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