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 |