NDC properties for "Humira Pen 40 MG/0.8 ML - Crohn's Disease Starter Pack" (RxCUI 825170)
About this data
The tables show NDC propoerties for Humira Pen 40 MG/0.8 ML - Crohn's Disease Starter Pack with the RxCUI 825170
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for Humira Pen 40 MG/0.8 ML - Crohn's Disease Starter Pack (RxCUI 825170)
| BLA | BLA125057 |
|---|---|
| MMSL_CODE | BD8853 |
| RxCUI | 825170 |
| SPL_SET_ID | 608d4f0d-b19f-46d3-749a-7159aa5f933d |
| Prescribable Synonym | Humira Pen 40 MG/0.8 ML - Crohn's Disease/Ulcerative Colitis Starter Pack |
| RXNAV_STR | Humira Pen 40 MG/0.8 ML - Crohn's Disease Starter Pack |
| RxNorm Name | {6 (0.8 ML adalimumab 50 MG/ML Auto-Injector [Humira]) } Pack [Humira Pen - Crohn's Disease Starter Pack] |
| RxNorm Synonym | Humira Pen 40 MG/0.8 ML - Crohn's Disease Starter Pack |
| RxNorm Synonym | Humira Pen 40 MG/0.8 ML - Crohn's Disease/Ulcerative Colitis Starter Pack |
| Related queries | Interactions (for RxCUI 825170) |
NDC Properties
NDC Item 00074433906
| NDC 9 | 0074-4339 |
|---|---|
| NDC 10 | 0074-4339-06 |
| NDC Item | 00074433906 |
| Packaging | 6 KIT in 1 CARTON (0074-4339-06) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .8 mL in 1 SYRINGE * 1 mL in 1 PACKET |
| BLA | BLA125057 |
| FDA SPL set id | 770190 |
| Labeler | AbbVie Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2006-06-23 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-4339 |
NDC Item 00074433973
| NDC 9 | 0074-4339 |
|---|---|
| NDC 10 | 0074-4339-73 |
| NDC Item | 00074433973 |
| Packaging | 6 KIT in 1 CARTON (0074-4339-73) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .8 mL in 1 SYRINGE * 1 mL in 1 PACKET |
| BLA | BLA125057 |
| FDA SPL set id | 770190 |
| Labeler | AbbVie Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2006-06-23 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-4339 |
NDC Item 00074433906
| NDC 9 | 0074-4339 |
|---|---|
| NDC 10 | 0074-4339-06 |
| NDC Item | 00074433906 |
| Packaging | 6 KIT in 1 CARTON (0074-4339-06) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .8 mL in 1 SYRINGE * 1 mL in 1 PACKET |
| BLA | BLA125057 |
| FDA SPL set id | 770190 |
| Labeler | AbbVie Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2006-06-23 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-4339 |
NDC Item 00074433973
| NDC 9 | 0074-4339 |
|---|---|
| NDC 10 | 0074-4339-73 |
| NDC Item | 00074433973 |
| Packaging | 6 KIT in 1 CARTON (0074-4339-73) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .8 mL in 1 SYRINGE * 1 mL in 1 PACKET |
| BLA | BLA125057 |
| FDA SPL set id | 770190 |
| Labeler | AbbVie Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2006-06-23 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-4339 |