NDC properties for "0.8 ML Humira 50 MG/ML Prefilled Syringe" (RxCUI 727705)
About this data
The tables show NDC propoerties for 0.8 ML Humira 50 MG/ML Prefilled Syringe with the RxCUI 727705
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 0.8 ML Humira 50 MG/ML Prefilled Syringe (RxCUI 727705)
| BLA | BLA125057 |
|---|---|
| MMSL_CODE | BD8853 |
| RxCUI | 727705 |
| SPL_SET_ID | 608d4f0d-b19f-46d3-749a-7159aa5f933d |
| Prescribable Synonym | Humira 40 MG in 0.8 ML Prefilled Syringe |
| RXNAV_STR | 0.8 ML Humira 50 MG/ML Prefilled Syringe |
| RxNorm Name | 0.8 ML adalimumab 50 MG/ML Prefilled Syringe [Humira] |
| RxNorm Synonym | 0.8 ML Humira 50 MG/ML Prefilled Syringe |
| RxNorm Synonym | Humira 40 MG per 0.8 ML Prefilled Syringe |
| Related queries | Interactions (for RxCUI 727705) |
NDC Properties
NDC Item 00074379902
| NDC 9 | 0074-3799 |
|---|---|
| NDC 10 | 0074-3799-02 |
| NDC Item | 00074379902 |
| Packaging | 2 KIT in 1 CARTON (0074-3799-02) / 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 | 2002-12-31 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-3799 |
NDC Item 00074379971
| NDC 9 | 0074-3799 |
|---|---|
| NDC 10 | 0074-3799-71 |
| NDC Item | 00074379971 |
| Packaging | 2 KIT in 1 CARTON (0074-3799-71) / 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 | 2002-12-31 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-3799 |
NDC Item 00074379902
| NDC 9 | 0074-3799 |
|---|---|
| NDC 10 | 0074-3799-02 |
| NDC Item | 00074379902 |
| Packaging | 2 KIT in 1 CARTON (0074-3799-02) / 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 | 2002-12-31 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-3799 |
NDC Item 00074379971
| NDC 9 | 0074-3799 |
|---|---|
| NDC 10 | 0074-3799-71 |
| NDC Item | 00074379971 |
| Packaging | 2 KIT in 1 CARTON (0074-3799-71) / 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 | 2002-12-31 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 0074-3799 |