Trulicity is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Dulaglutide.
Product ID | 50090-3483_4b0fc2d3-dd98-43f2-b5a1-ad66a07ebaaa |
NDC | 50090-3483 |
Product Type | Human Prescription Drug |
Proprietary Name | Trulicity |
Generic Name | Dulaglutide |
Dosage Form | Injection, Solution |
Route of Administration | SUBCUTANEOUS |
Marketing Start Date | 2014-09-18 |
Marketing Category | BLA / BLA |
Application Number | BLA125469 |
Labeler Name | A-S Medication Solutions |
Substance Name | DULAGLUTIDE |
Active Ingredient Strength | 2 mg/.5mL |
Pharm Classes | GLP-1 Receptor Agonist [EPC],Glucagon-Like Peptide 1 [CS],Glucagon-like Peptide-1 (GLP-1) Agonists [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2018-06-18 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA125469 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-06-18 |
Marketing End Date | 2019-11-30 |
Ingredient | Strength |
---|---|
DULAGLUTIDE | 1.5 mg/.5mL |
SPL SET ID: | 58353438-3236-4596-9324-62fed9615cb7 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0002-1433 | Trulicity | Dulaglutide |
0002-1434 | Trulicity | Dulaglutide |
0002-2236 | Trulicity | Dulaglutide |
0002-3182 | Trulicity | Dulaglutide |
50090-3483 | Trulicity | Dulaglutide |
50090-3484 | Trulicity | Trulicity |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRULICITY 86315558 not registered Dead/Abandoned |
Eli Lilly and Company 2014-06-20 |
TRULICITY 86314558 not registered Dead/Abandoned |
Eli Lilly and Company 2014-06-19 |
TRULICITY 86271432 5069090 Live/Registered |
Eli Lilly and Company 2014-05-05 |
TRULICITY 85183667 4786025 Live/Registered |
Eli Lilly and Company 2010-11-23 |