CYRAMZA is a Intravenous Solution in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is Ramucirumab.
| Product ID | 0002-7669_07c65766-dcfd-4196-bd57-b21abf44815d | 
| NDC | 0002-7669 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | CYRAMZA | 
| Generic Name | Ramucirumab | 
| Dosage Form | Solution | 
| Route of Administration | INTRAVENOUS | 
| Marketing Start Date | 2014-04-21 | 
| Marketing Category | BLA / BLA | 
| Application Number | BLA125477 | 
| Labeler Name | Eli Lilly and Company | 
| Substance Name | RAMUCIRUMAB | 
| Active Ingredient Strength | 10 mg/mL | 
| Pharm Classes | VEGFR2 Inhibitors [MoA], Vascular Endothelial Growth Factor Receptor 2 Antagonist [EPC] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2023-12-31 | 
| Marketing Start Date | 2014-04-21 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | BLA | 
| Application Number | BLA125477 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | ML | 
| Marketing Start Date | 2014-04-21 | 
| Ingredient | Strength | 
|---|---|
| RAMUCIRUMAB | 10 mg/mL | 
| SPL SET ID: | c6080942-dee6-423e-b688-1272c2ae90d4 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0002-7669 | CYRAMZA | ramucirumab | 
| 0002-7678 | CYRAMZA | ramucirumab | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() CYRAMZA  86315717  4899164 Live/Registered  | 
        ImClone LLC  2014-06-20  | 
![]() CYRAMZA  86241873  not registered Dead/Abandoned  | 
        ImClone LLC  2014-04-03  | 
![]() CYRAMZA  85447460  4580501 Live/Registered  | 
        ImClone LLC  2011-10-14  |