Humira is a Kit in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is .
Product ID | 0074-2540_05cc7e8b-7ac7-6196-0260-f15f8aad95ba |
NDC | 0074-2540 |
Product Type | Human Prescription Drug |
Proprietary Name | Humira |
Generic Name | Adalimumab |
Dosage Form | Kit |
Marketing Start Date | 2016-10-17 |
Marketing Category | BLA / BLA |
Application Number | BLA125057 |
Labeler Name | AbbVie Inc. |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2016-10-17 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA125057 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-10-17 |
Marketing Category | BLA |
Application Number | BLA125057 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-10-17 |
SPL SET ID: | 608d4f0d-b19f-46d3-749a-7159aa5f933d |
Manufacturer | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0074-0067 | Humira | Adalimumab |
0074-0124 | Humira | Adalimumab |
0074-0243 | Humira | Adalimumab |
0074-0554 | Humira | Adalimumab |
0074-0616 | Humira | Adalimumab |
0074-0817 | Humira | Humira |
0074-2540 | Humira | Humira |
0074-1539 | Humira | Humira |
0074-4339 | Humira | Humira |
0074-3799 | Humira | Humira |
0074-9374 | Humira | Humira |
0074-6347 | Humira | Humira |
50090-3530 | Humira | Humira |
50090-4487 | Humira | Humira |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HUMIRA 78082476 2725934 Live/Registered |
ABBVIE BIOTECHNOLOGY LTD. 2001-09-04 |
HUMIRA 77831297 3784305 Live/Registered |
ABBVIE BIOTECHNOLOGY LTD. 2009-09-21 |