Product Details

AVASTIN 400 MG/16 ML VIAL

Manufacturer: GENENTECH, INC

MFG#: 50242-0061-01

NDC: 50242-0061-01

PID: 636512

1/UN

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Product Information

NDC Package Code50242-061-01
Proprietary NameAvastin
Non-Proprietary NameBevacizumab
Package1 VIAL, SINGLE-USE in 1 CARTON (50242-061-01) > 16 mL in 1 VIAL, SINGLE-USE
Dosage FormINJECTION, SOLUTION
RouteINTRAVENOUS
Active Ingredient Strength400
Active Ingredient Unitsmg/16mL
Substance NameBEVACIZUMAB

Description

Avastin is a vascular endothelial growth factor inhibitor indicated for the treatment of: 1 Metastatic colorectal cancer, in combination with intravenous fluorouracil-based chemotherapy for first- or second-line treatment. (1.1), 2 Metastatic colorectal cancer, in combination with fluoropyrimidine-irinotecan- or fluoropyrimidine-oxaliplatin-based chemotherapy for second-line treatment in patients who have progressed on a first-line bevacizumab product-containing regimen. (1.1).

Bevacizumab is a vascular endothelial growth factor inhibitor. Bevacizumab is a recombinant humanized monoclonal IgG1 antibody that contains human framework regions and murine complementarity-determining regions. Bevacizumab has an approximate molecular weight of 149 kDa. Bevacizumab is produced in a mammalian cell (Chinese Hamster Ovary) expression system. Avastin (bevacizumab) injection is a sterile, preservative-free, clear to slightly opalescent, colorless to pale brown solution in a single-dose vial for intravenous use. Avastin contains bevacizumab at a concentration of 25 mg/mL in either a 100 mg/4 mL or 400 mg/16 mL single-dose vial. Each mL of solution contains 25 mg bevacizumab, a,a-trehalose dihydrate (60 mg), polysorbate 20 (0.4 mg), sodium phosphate dibasic, anhydrous (1.2 mg), sodium phosphate monobasic, monohydrate (5.8 mg), and Water for Injection, USP. The pH is 6.2.

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AVASTIN 400 MG/16 ML VIAL is manufactured by GENENTECH, INC.

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