NDC properties for "0.8 ML Hadlima 50 MG/ML Auto-Injector" (RxCUI 2640300)
About this data
The tables show NDC propoerties for 0.8 ML Hadlima 50 MG/ML Auto-Injector with the RxCUI 2640300
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 Hadlima 50 MG/ML Auto-Injector (RxCUI 2640300)
| BLA | BLA761059 |
|---|---|
| MMSL_CODE | BD35654 |
| RxCUI | 2640300 |
| SPL_SET_ID | 4774a951-3ce8-43b6-80b1-e6b23752aae6 |
| SPL_SET_ID | ef25af7e-6267-409a-8d68-de51eb48812a |
| Prescribable Synonym | HADLIMA 40 MG in 0.8 ML Auto-Injector |
| RXNAV_STR | 0.8 ML Hadlima 50 MG/ML Auto-Injector |
| RxNorm Name | 0.8 ML adalimumab-bwwd 50 MG/ML Auto-Injector [Hadlima] |
| RxNorm Synonym | 0.8 ML Hadlima 50 MG/ML Auto-Injector |
| RxNorm Synonym | Hadlima 40 MG per 0.8 ML Auto-Injector |
| Related queries | Interactions (for RxCUI 2640300) |
NDC Properties
NDC Item 50090670600
| NDC 9 | 50090-6706 |
|---|---|
| NDC 10 | 50090-6706-0 |
| NDC Item | 50090670600 |
| Packaging | 2 CARTON in 1 CARTON (50090-6706-0) / 1 mL in 1 CARTON |
| BLA | BLA761059 |
| FDA SPL set id | 732868 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 50090-6706 |
NDC Item 78206018401
| NDC 9 | 78206-184 |
|---|---|
| NDC 10 | 78206-184-01 |
| NDC Item | 78206018401 |
| Packaging | 2 CARTON in 1 CARTON (78206-184-01) / 1 SYRINGE in 1 CARTON (78206-184-99) / .8 mL in 1 SYRINGE |
| BLA | BLA761059 |
| FDA SPL set id | 796818 |
| Labeler | Organon LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 78206-184 |
NDC Item 78206018499
| NDC 9 | 78206-184 |
|---|---|
| NDC 10 | 78206-184-99 |
| NDC Item | 78206018499 |
| Packaging | 0.8 mL in 1 SYRINGE |
| Packaging | 1 in 1 CARTON |
| BLA | BLA761059 |
| FDA SPL set id | 796818 |
| Labeler | Organon LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 78206-184 |
NDC Item 50090670600
| NDC 9 | 50090-6706 |
|---|---|
| NDC 10 | 50090-6706-0 |
| NDC Item | 50090670600 |
| Packaging | 2 CARTON in 1 CARTON (50090-6706-0) / 1 mL in 1 CARTON |
| BLA | BLA761059 |
| FDA SPL set id | 732868 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 50090-6706 |
NDC Item 78206018401
| NDC 9 | 78206-184 |
|---|---|
| NDC 10 | 78206-184-01 |
| NDC Item | 78206018401 |
| Packaging | 2 CARTON in 1 CARTON (78206-184-01) / 1 SYRINGE in 1 CARTON (78206-184-99) / .8 mL in 1 SYRINGE |
| BLA | BLA761059 |
| FDA SPL set id | 796818 |
| Labeler | Organon LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 78206-184 |
NDC Item 78206018499
| NDC 9 | 78206-184 |
|---|---|
| NDC 10 | 78206-184-99 |
| NDC Item | 78206018499 |
| Packaging | 0.8 mL in 1 SYRINGE |
| Packaging | 1 in 1 CARTON |
| BLA | BLA761059 |
| FDA SPL set id | 796818 |
| Labeler | Organon LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 78206-184 |
NDC Item 50090670600
| NDC 9 | 50090-6706 |
|---|---|
| NDC 10 | 50090-6706-0 |
| NDC Item | 50090670600 |
| Packaging | 2 CARTON in 1 CARTON (50090-6706-0) / 1 mL in 1 CARTON |
| BLA | BLA761059 |
| FDA SPL set id | 732868 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 50090-6706 |
NDC Item 78206018401
| NDC 9 | 78206-184 |
|---|---|
| NDC 10 | 78206-184-01 |
| NDC Item | 78206018401 |
| Packaging | 2 CARTON in 1 CARTON (78206-184-01) / 1 SYRINGE in 1 CARTON (78206-184-99) / .8 mL in 1 SYRINGE |
| BLA | BLA761059 |
| FDA SPL set id | 796818 |
| Labeler | Organon LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 78206-184 |
NDC Item 78206018499
| NDC 9 | 78206-184 |
|---|---|
| NDC 10 | 78206-184-99 |
| NDC Item | 78206018499 |
| Packaging | 0.8 mL in 1 SYRINGE |
| Packaging | 1 in 1 CARTON |
| BLA | BLA761059 |
| FDA SPL set id | 796818 |
| Labeler | Organon LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2023-07-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 78206-184 |