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Kineret
Kineret - 66658-234-28 - (anakinra)
Drug Information of Kineret
| Product NDC: | 66658-234 |
| Proprietary Name: | Kineret |
| Non Proprietary Name: | anakinra |
| Active Ingredient(s): | 100 mg/.67mL & nbsp; anakinra |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kineret
| Product NDC: | 66658-234 |
| Labeler Name: | Swedish Orphan Biovitrum AB (publ) |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103950 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20091215 |
Package Information of Kineret
| Package NDC: | 66658-234-28 |
| Package Description: | 4 CARTON in 1 CASE (66658-234-28) > 7 SYRINGE, GLASS in 1 CARTON (66658-234-07) > .67 mL in 1 SYRINGE, GLASS (66658-234-01) |
NDC Information of Kineret
| NDC Code | 66658-234-28 |
| Proprietary Name | Kineret |
| Package Description | 4 CARTON in 1 CASE (66658-234-28) > 7 SYRINGE, GLASS in 1 CARTON (66658-234-07) > .67 mL in 1 SYRINGE, GLASS (66658-234-01) |
| Product NDC | 66658-234 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | anakinra |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20091215 |
| Marketing Category Name | BLA |
| Labeler Name | Swedish Orphan Biovitrum AB (publ) |
| Substance Name | ANAKINRA |
| Strength Number | 100 |
| Strength Unit | mg/.67mL |
| Pharmaceutical Classes | Interleukin 1 Receptor Antagonists [MoA],Interleukin-1 Receptor Antagonist [EPC] |
