Eptifibatide (Teva Parenteral Medicines, Inc.)
Welcome to the PulseAid listing for the Eptifibatide drug offered from Teva Parenteral Medicines, Inc.. This Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [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: | Eptifibatide |
| SUBSTANCE NAME: | EPTIFIBATIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-07-06 |
| END MARKETING DATE: | 0000-00-00 |
Eptifibatide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Eptifibatide from Teva Parenteral Medicines, Inc. |
| LABELER NAME: | Teva Parenteral Medicines, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2(mg/mL) |
| START MARKETING DATE: | 2016-07-06 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0703-1165_bd9c2668-0e91-44b2-8205-bdd8f82fa5c3 |
| PRODUCT NDC: | 0703-1165 |
| APPLICATION NUMBER: | ANDA090854 |
Other EPTIFIBATIDE Pharmaceutical Manufacturers / Labelers: