NDC properties for "Humira Pen 80 MG/0.8 ML - Starter Package for Crohn's Disease, Ulcerative Colitis or Hidradenitis Suppurativa (3 count)" (RxCUI 1921245)
About this data
The tables show NDC propoerties for Humira Pen 80 MG/0.8 ML - Starter Package for Crohn's Disease, Ulcerative Colitis or Hidradenitis Suppurativa (3 count) with the RxCUI 1921245
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 80 MG/0.8 ML - Starter Package for Crohn's Disease, Ulcerative Colitis or Hidradenitis Suppurativa (3 count) (RxCUI 1921245)
BLA | BLA125057 |
---|---|
MMSL_CODE | BD32944 |
RxCUI | 1921245 |
SPL_SET_ID | 608d4f0d-b19f-46d3-749a-7159aa5f933d |
Prescribable Synonym | Humira Pen 80 MG/0.8 ML - Starter Package for Crohn's Disease, Ulcerative Colitis or Hidradenitis Suppurativa (3 count) |
RXNAV_STR | Humira Pen 80 MG/0.8 ML - Starter Package for Crohn's Disease, Ulcerative Colitis or Hidradenitis Suppurativa (3 count) |
RxNorm Name | {3 (0.8 ML adalimumab 100 MG/ML Auto-Injector [Humira]) } Pack [Humira Pen 80 MG/0.8 ML - Starter Package for Crohn's Disease, Ulcerative Colitis or Hidradenitis Suppurativa] |
RxNorm Synonym | Humira Pen 80 MG/0.8 ML - Starter Package for Crohn's Disease, Ulcerative Colitis or Hidradenitis Suppurativa (3 count) |
Related queries | Interactions (for RxCUI 1921245) |
NDC Properties
NDC Item 00074012403
NDC 9 | 0074-0124 |
---|---|
NDC 10 | 0074-0124-03 |
NDC Item | 00074012403 |
Packaging | 3 KIT in 1 CARTON (0074-0124-03) / 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 | 2017-04-21 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 0074-0124 |
NDC Item 00074012473
NDC 9 | 0074-0124 |
---|---|
NDC 10 | 0074-0124-73 |
NDC Item | 00074012473 |
Packaging | 3 KIT in 1 CARTON (0074-0124-73) / 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 | 2017-04-21 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 0074-0124 |
NDC Item 00074012403
NDC 9 | 0074-0124 |
---|---|
NDC 10 | 0074-0124-03 |
NDC Item | 00074012403 |
Packaging | 3 KIT in 1 CARTON (0074-0124-03) / 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 | 2017-04-21 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 0074-0124 |
NDC Item 00074012473
NDC 9 | 0074-0124 |
---|---|
NDC 10 | 0074-0124-73 |
NDC Item | 00074012473 |
Packaging | 3 KIT in 1 CARTON (0074-0124-73) / 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 | 2017-04-21 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 0074-0124 |