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Lantus
Lantus - 0088-2219-05 - (insulin glargine)
Drug Information of Lantus
| Product NDC: | 0088-2219 |
| Proprietary Name: | Lantus |
| Non Proprietary Name: | insulin glargine |
| Active Ingredient(s): | 100 [iU]/mL & nbsp; insulin glargine |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lantus
| Product NDC: | 0088-2219 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021081 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090923 |
Package Information of Lantus
| Package NDC: | 0088-2219-05 |
| Package Description: | 5 CARTRIDGE in 1 CARTON (0088-2219-05) > 3 mL in 1 CARTRIDGE |
NDC Information of Lantus
| NDC Code | 0088-2219-05 |
| Proprietary Name | Lantus |
| Package Description | 5 CARTRIDGE in 1 CARTON (0088-2219-05) > 3 mL in 1 CARTRIDGE |
| Product NDC | 0088-2219 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | insulin glargine |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20090923 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | INSULIN GLARGINE |
| Strength Number | 100 |
| Strength Unit | [iU]/mL |
| Pharmaceutical Classes | Insulin [Chemical/Ingredient],Insulin Analog [EPC] |
