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Cimzia
Cimzia - 50474-710-81 - (certolizumab pegol)
Drug Information of Cimzia
| Product NDC: | 50474-710 |
| Proprietary Name: | Cimzia |
| Non Proprietary Name: | certolizumab pegol |
| Active Ingredient(s): | 200 mg/mL & nbsp; certolizumab pegol |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cimzia
| Product NDC: | 50474-710 |
| Labeler Name: | UCB, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125160 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20090514 |
Package Information of Cimzia
| Package NDC: | 50474-710-81 |
| Package Description: | 3 CARTON in 1 BOX (50474-710-81) > 2 SYRINGE, GLASS in 1 CARTON > 1 mL in 1 SYRINGE, GLASS |
NDC Information of Cimzia
| NDC Code | 50474-710-81 |
| Proprietary Name | Cimzia |
| Package Description | 3 CARTON in 1 BOX (50474-710-81) > 2 SYRINGE, GLASS in 1 CARTON > 1 mL in 1 SYRINGE, GLASS |
| Product NDC | 50474-710 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | certolizumab pegol |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20090514 |
| Marketing Category Name | BLA |
| Labeler Name | UCB, Inc. |
| Substance Name | CERTOLIZUMAB PEGOL |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
