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ORENCIA
ORENCIA - 0003-2188-41 - (abatacept)
Drug Information of ORENCIA
| Product NDC: | 0003-2188 |
| Proprietary Name: | ORENCIA |
| Non Proprietary Name: | abatacept |
| Active Ingredient(s): | 125 mg/mL & nbsp; abatacept |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ORENCIA
| Product NDC: | 0003-2188 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125118 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20110729 |
Package Information of ORENCIA
| Package NDC: | 0003-2188-41 |
| Package Description: | 1 SYRINGE, GLASS in 1 CARTON (0003-2188-41) > 1 mL in 1 SYRINGE, GLASS |
NDC Information of ORENCIA
| NDC Code | 0003-2188-41 |
| Proprietary Name | ORENCIA |
| Package Description | 1 SYRINGE, GLASS in 1 CARTON (0003-2188-41) > 1 mL in 1 SYRINGE, GLASS |
| Product NDC | 0003-2188 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | abatacept |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20110729 |
| Marketing Category Name | BLA |
| Labeler Name | E.R. Squibb & Sons, L.L.C. |
| Substance Name | ABATACEPT |
| Strength Number | 125 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Cytokine Activity [PE],Selective T Cell Costimulation Modulator [EPC],Recombinant Fusion Proteins [Chemical/Ingredient] |
