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Kalbitor
Kalbitor - 47783-101-01 - (ecallantide)
Drug Information of Kalbitor
| Product NDC: | 47783-101 |
| Proprietary Name: | Kalbitor |
| Non Proprietary Name: | ecallantide |
| Active Ingredient(s): | 10 mg/mL & nbsp; ecallantide |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kalbitor
| Product NDC: | 47783-101 |
| Labeler Name: | Dyax Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125277 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20100201 |
Package Information of Kalbitor
| Package NDC: | 47783-101-01 |
| Package Description: | 1 BOX in 1 CARTON (47783-101-01) > 3 VIAL in 1 BOX > 1 mL in 1 VIAL |
NDC Information of Kalbitor
| NDC Code | 47783-101-01 |
| Proprietary Name | Kalbitor |
| Package Description | 1 BOX in 1 CARTON (47783-101-01) > 3 VIAL in 1 BOX > 1 mL in 1 VIAL |
| Product NDC | 47783-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ecallantide |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20100201 |
| Marketing Category Name | BLA |
| Labeler Name | Dyax Corp. |
| Substance Name | ECALLANTIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
