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Levemir
Levemir - 0169-6439-10 - (insulin detemir)
Drug Information of Levemir
| Product NDC: | 0169-6439 |
| Proprietary Name: | Levemir |
| Non Proprietary Name: | insulin detemir |
| Active Ingredient(s): | 14.2 mg/mL & nbsp; insulin detemir |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levemir
| Product NDC: | 0169-6439 |
| Labeler Name: | Novo Nordisk |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021536 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060327 |
Package Information of Levemir
| Package NDC: | 0169-6439-10 |
| Package Description: | 5 SYRINGE, PLASTIC in 1 CARTON (0169-6439-10) > 3 mL in 1 SYRINGE, PLASTIC |
NDC Information of Levemir
| NDC Code | 0169-6439-10 |
| Proprietary Name | Levemir |
| Package Description | 5 SYRINGE, PLASTIC in 1 CARTON (0169-6439-10) > 3 mL in 1 SYRINGE, PLASTIC |
| Product NDC | 0169-6439 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | insulin detemir |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20060327 |
| Marketing Category Name | NDA |
| Labeler Name | Novo Nordisk |
| Substance Name | INSULIN DETEMIR |
| Strength Number | 14.2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Insulin [Chemical/Ingredient],Insulin Analog [EPC] |
