Lantus (sanofi-aventis U.S. LLC)
Welcome to the PulseAid listing for the Lantus drug offered from sanofi-aventis U.S. LLC. This Insulin [Chemical/Ingredient],Insulin Analog [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | sanofi-aventis U.S. LLC |
| NON-PROPRIETARY NAME: | insulin glargine |
| SUBSTANCE NAME: | INSULIN GLARGINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Insulin [Chemical/Ingredient],Insulin Analog [EPC] |
| ROUTE: | SUBCUTANEOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2009-09-23 |
| END MARKETING DATE: | 0000-00-00 |
Lantus HUMAN PRESCRIPTION DRUG Details:
| Item Description | Lantus from sanofi-aventis U.S. LLC |
| LABELER NAME: | sanofi-aventis U.S. LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 100([iU]/mL) |
| START MARKETING DATE: | 2009-09-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0088-2220_0dd5b537-70f4-45d3-8003-8ce600908e96 |
| PRODUCT NDC: | 0088-2220 |
| APPLICATION NUMBER: | NDA021081 |
Other INSULIN GLARGINE Pharmaceutical Manufacturers / Labelers:
