Epoprostenol Sodium (Teva Parenteral Medicines, Inc.)
Welcome to the PulseAid listing for the Epoprostenol Sodium drug offered from Teva Parenteral Medicines, Inc.. This Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE] 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: | Epoprostenol Sodium |
| SUBSTANCE NAME: | EPOPROSTENOL SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Prostacycline Vasodilator [EPC],Prostaglandins I [Chemical/Ingredient],Vasodilation [PE] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, POWDER, FOR SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2008-04-23 |
| END MARKETING DATE: | 0000-00-00 |
Epoprostenol Sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Epoprostenol Sodium from Teva Parenteral Medicines, Inc. |
| LABELER NAME: | Teva Parenteral Medicines, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.5(mg/1) |
| START MARKETING DATE: | 2008-04-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0703-1985_45b8b475-ff2a-40c1-b330-0db3934d3e43 |
| PRODUCT NDC: | 0703-1985 |
| APPLICATION NUMBER: | ANDA078396 |
Other EPOPROSTENOL SODIUM Pharmaceutical Manufacturers / Labelers:
