Liothyronine Sodium (PD-Rx Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Liothyronine Sodium drug offered from PD-Rx Pharmaceuticals, Inc.. This l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient] 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: | PD-Rx Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Liothyronine Sodium |
| SUBSTANCE NAME: | LIOTHYRONINE SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2009-03-23 |
| END MARKETING DATE: | 0000-00-00 |
Liothyronine Sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Liothyronine Sodium from PD-Rx Pharmaceuticals, Inc. |
| LABELER NAME: | PD-Rx Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(ug/1) |
| START MARKETING DATE: | 2009-03-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 43063-252_518dfa79-2401-2bce-e054-00144ff88e88 |
| PRODUCT NDC: | 43063-252 |
| APPLICATION NUMBER: | ANDA090097 |
Other LIOTHYRONINE SODIUM Pharmaceutical Manufacturers / Labelers:
