Heparin Sodium and Sodium Chloride (Baxter Healthcare Corporation)
Welcome to the PulseAid listing for the Heparin Sodium and Sodium Chloride drug offered from Baxter Healthcare Corporation. This Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated 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: | Baxter Healthcare Corporation |
| NON-PROPRIETARY NAME: | HEPARIN SODIUM |
| SUBSTANCE NAME: | HEPARIN SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1982-04-28 |
| END MARKETING DATE: | 0000-00-00 |
Heparin Sodium and Sodium Chloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Heparin Sodium and Sodium Chloride from Baxter Healthcare Corporation |
| LABELER NAME: | Baxter Healthcare Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 200([USP’U]/100mL) |
| START MARKETING DATE: | 1982-04-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0338-0431_9930df8e-e1d7-495f-8f68-9a96604164f5 |
| PRODUCT NDC: | 0338-0431 |
| APPLICATION NUMBER: | NDA018609 |
Other HEPARIN SODIUM Pharmaceutical Manufacturers / Labelers:
