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Simponi
Simponi - 57894-070-01 - (golimumab)
Drug Information of Simponi
| Product NDC: | 57894-070 |
| Proprietary Name: | Simponi |
| Non Proprietary Name: | golimumab |
| Active Ingredient(s): | 50 mg/.5mL & nbsp; golimumab |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Simponi
| Product NDC: | 57894-070 |
| Labeler Name: | Janssen Biotech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125289 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20090425 |
Package Information of Simponi
| Package NDC: | 57894-070-01 |
| Package Description: | 1 SYRINGE, GLASS in 1 CARTON (57894-070-01) > .5 mL in 1 SYRINGE, GLASS |
NDC Information of Simponi
| NDC Code | 57894-070-01 |
| Proprietary Name | Simponi |
| Package Description | 1 SYRINGE, GLASS in 1 CARTON (57894-070-01) > .5 mL in 1 SYRINGE, GLASS |
| Product NDC | 57894-070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | golimumab |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20090425 |
| Marketing Category Name | BLA |
| Labeler Name | Janssen Biotech, Inc. |
| Substance Name | GOLIMUMAB |
| Strength Number | 50 |
| Strength Unit | mg/.5mL |
| Pharmaceutical Classes | Tumor Necrosis Factor Blocker [EPC] |
