Product NDC: | 0088-2500 |
Proprietary Name: | Apidra |
Non Proprietary Name: | insulin glulisine |
Active Ingredient(s): | 100 [iU]/mL & nbsp; insulin glulisine |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0088-2500 |
Labeler Name: | Sanofi-Aventis U.S. LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021629 |
Marketing Category: | NDA |
Start Marketing Date: | 20090224 |
Package NDC: | 0088-2500-33 |
Package Description: | 10 mL in 1 VIAL, GLASS (0088-2500-33) |
NDC Code | 0088-2500-33 |
Proprietary Name | Apidra |
Package Description | 10 mL in 1 VIAL, GLASS (0088-2500-33) |
Product NDC | 0088-2500 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | insulin glulisine |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 20090224 |
Marketing Category Name | NDA |
Labeler Name | Sanofi-Aventis U.S. LLC |
Substance Name | INSULIN GLULISINE |
Strength Number | 100 |
Strength Unit | [iU]/mL |
Pharmaceutical Classes | Insulin [Chemical/Ingredient],Insulin Analog [EPC] |