Avastin is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Genentech, Inc.. The primary component is Bevacizumab.
Product ID | 50242-061_3580958a-7a01-45c0-8d9c-87d9a3963158 |
NDC | 50242-061 |
Product Type | Human Prescription Drug |
Proprietary Name | Avastin |
Generic Name | Bevacizumab |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2004-02-26 |
Marketing Category | BLA / BLA |
Application Number | BLA125085 |
Labeler Name | Genentech, Inc. |
Substance Name | BEVACIZUMAB |
Active Ingredient Strength | 400 mg/16mL |
Pharm Classes | Vascular Endothelial Growth Factor Inhibitor [EPC], Vascular Endothelial Growth Factor Inhibitors [MoA], Vascular Endothelial Growth Factor-directed Antibody Interactions [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2004-02-26 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA125085 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-04-01 |
Marketing Category | BLA |
Application Number | BLA125085 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2004-02-26 |
Ingredient | Strength |
---|---|
BEVACIZUMAB | 400 mg/16mL |
SPL SET ID: | 939b5d1f-9fb2-4499-80ef-0607aa6b114e |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
50242-060 | Avastin | bevacizumab |
50242-061 | Avastin | bevacizumab |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AVASTIN 76278294 2981298 Live/Registered |
GENENTECH, INC. 2001-06-29 |