NDC properties for "adalimumab-aacf 40 MG per 0.8 ML Auto-Injector" (RxCUI 2640859)
About this data
The tables show NDC propoerties for adalimumab-aacf 40 MG per 0.8 ML Auto-Injector with the RxCUI 2640859
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 adalimumab-aacf 40 MG per 0.8 ML Auto-Injector (RxCUI 2640859)
| BLA | BLA761255 |
|---|---|
| MMSL_CODE | BD39074 |
| RxCUI | 2640859 |
| SPL_SET_ID | 2488b0bc-7b8f-4cc8-91ea-48e7ea5e8915 |
| VUID | 4042367 |
| Prescribable Synonym | adalimumab-aacf 40 MG in 0.8 ML Auto-Injector |
| RXNAV_STR | 0.8 ML adalimumab-aacf 50 MG/ML Auto-Injector |
| RxNorm Name | 0.8 ML adalimumab-aacf 50 MG/ML Auto-Injector |
| RxNorm Synonym | adalimumab-aacf 40 MG per 0.8 ML Auto-Injector |
| Related queries | Interactions (for RxCUI 2640859) |
NDC Properties
NDC Item 65219061002
| NDC 9 | 65219-610 |
|---|---|
| NDC 10 | 65219-610-02 |
| NDC Item | 65219061002 |
| Packaging | 0.8 mL in 1 SYRINGE, GLASS |
| FDA SPL set id | 752075 |
| Labeler | Fresenius Kabi USA, LLC |
| Label type | HUMAN PRESCRIPTION DRUG LABEL |
| Related queries | Properties for NDC 9 65219-610 |
NDC Item 65219061299
| NDC 9 | 65219-612 |
|---|---|
| NDC 10 | 65219-612-99 |
| NDC Item | 65219061299 |
| Packaging | 1 KIT in 1 CARTON (65219-612-99) * .8 mL in 1 SYRINGE, GLASS (65219-610-02) * 1 SWAB in 1 POUCH (65219-332-95) |
| BLA | BLA761255 |
| FDA SPL set id | 752075 |
| Labeler | Fresenius Kabi USA, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-12-06 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 65219-612 |
NDC Item 65219061002
| NDC 9 | 65219-610 |
|---|---|
| NDC 10 | 65219-610-02 |
| NDC Item | 65219061002 |
| Packaging | 0.8 mL in 1 SYRINGE, GLASS |
| FDA SPL set id | 752075 |
| Labeler | Fresenius Kabi USA, LLC |
| Label type | HUMAN PRESCRIPTION DRUG LABEL |
| Related queries | Properties for NDC 9 65219-610 |
NDC Item 65219061299
| NDC 9 | 65219-612 |
|---|---|
| NDC 10 | 65219-612-99 |
| NDC Item | 65219061299 |
| Packaging | 1 KIT in 1 CARTON (65219-612-99) * .8 mL in 1 SYRINGE, GLASS (65219-610-02) * 1 SWAB in 1 POUCH (65219-332-95) |
| BLA | BLA761255 |
| FDA SPL set id | 752075 |
| Labeler | Fresenius Kabi USA, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-12-06 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 65219-612 |