Enoxaparin Sodium (Teva Parenteral Medicines, Inc.)
Welcome to the PulseAid listing for the Enoxaparin Sodium drug offered from Teva Parenteral Medicines, Inc.. This Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [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: | Teva Parenteral Medicines, Inc. |
| NON-PROPRIETARY NAME: | Enoxaparin Sodium |
| SUBSTANCE NAME: | ENOXAPARIN SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] |
| ROUTE: | INTRAVENOUS; SUBCUTANEOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-02-19 |
| END MARKETING DATE: | 0000-00-00 |
Enoxaparin Sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Enoxaparin Sodium from Teva Parenteral Medicines, Inc. |
| LABELER NAME: | Teva Parenteral Medicines, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 150(mg/mL) |
| START MARKETING DATE: | 2015-02-19 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0703-8510_be8aaa0a-dd91-4f55-a5d5-c0290230a228 |
| PRODUCT NDC: | 0703-8510 |
| APPLICATION NUMBER: | ANDA076726 |
Other ENOXAPARIN SODIUM Pharmaceutical Manufacturers / Labelers: