REPATHA is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Amgen Inc. The primary component is Evolocumab.
| Product ID | 55513-750_02a067d5-ee1b-4d79-aea5-d0e843246a64 |
| NDC | 55513-750 |
| Product Type | Human Prescription Drug |
| Proprietary Name | REPATHA |
| Generic Name | Evolocumab |
| Dosage Form | Injection, Solution |
| Route of Administration | SUBCUTANEOUS |
| Marketing Start Date | 2015-08-31 |
| Marketing Category | BLA / BLA |
| Application Number | BLA125522 |
| Labeler Name | Amgen Inc |
| Substance Name | EVOLOCUMAB |
| Active Ingredient Strength | 140 mg/mL |
| Pharm Classes | PCSK9 Inhibitor [EPC],PCSK9 Inhibitors [MoA],Antibodies, Monoclonal [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2015-08-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA125522 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2015-08-31 |
| Ingredient | Strength |
|---|---|
| EVOLOCUMAB | 140 mg/mL |
| SPL SET ID: | 709338ae-ab8f-44a9-b7d5-abaabec3493a |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 55513-750 | REPATHA | Evolocumab |
| 55513-760 | REPATHA | Evolocumab |
| 55513-770 | REPATHA | Evolocumab |
| 72511-750 | REPATHA | Evolocumab |
| 72511-760 | REPATHA | Evolocumab |
| 72511-770 | REPATHA | REPATHA |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() REPATHA 86436098 not registered Dead/Abandoned |
Amgen Inc. 2014-10-27 |
![]() REPATHA 86066934 4837298 Live/Registered |
Amgen Inc. 2013-09-17 |
![]() REPATHA 76463628 not registered Dead/Abandoned |
Amgen Inc. 2002-11-01 |