ACTIMMUNE is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Horizon Therapeutics Usa, Inc.. The primary component is Interferon Gamma-1b.
Product ID | 75987-111_10c38fa8-bbf3-40e5-83dc-bc105723a442 |
NDC | 75987-111 |
Product Type | Human Prescription Drug |
Proprietary Name | ACTIMMUNE |
Generic Name | Interferon Gamma-1b |
Dosage Form | Injection, Solution |
Route of Administration | SUBCUTANEOUS |
Marketing Start Date | 2013-12-01 |
Marketing Category | BLA / BLA |
Application Number | BLA103836 |
Labeler Name | Horizon Therapeutics USA, Inc. |
Substance Name | INTERFERON GAMMA-1B |
Active Ingredient Strength | 100 ug/.5mL |
Pharm Classes | Interferon gamma [EPC],Interferon-gamma [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2013-12-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA103836 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2013-12-01 |
Marketing Category | BLA |
Application Number | BLA103836 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2013-12-01 |
Ingredient | Strength |
---|---|
INTERFERON GAMMA-1B | 100 ug/.5mL |
SPL SET ID: | 5d0b1256-1981-4519-94f4-a4a2f98bd8a3 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
75987-111 | ACTIMMUNE | Interferon gamma-1b |
17089-378 | GUNA-INF GAMMA | INTERFERON GAMMA-1B |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACTIMMUNE 77792019 not registered Dead/Abandoned |
Active Organics, Inc. 2009-07-29 |
ACTIMMUNE 75473512 not registered Dead/Abandoned |
Legacy Health International, Inc. 1998-04-24 |
ACTIMMUNE 73796028 1617288 Live/Registered |
GENENTECH, INC. 1989-04-26 |