MoviPrep (Salix Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the MoviPrep drug offered from Salix Pharmaceuticals, Inc.. This 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: | Salix Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2006-10-01 |
| END MARKETING DATE: | 0000-00-00 |
MoviPrep HUMAN PRESCRIPTION DRUG Details:
| Item Description | MoviPrep from Salix Pharmaceuticals, Inc. |
| LABELER NAME: | Salix Pharmaceuticals, Inc. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2006-10-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 65649-201_7a33061d-935f-4b5b-b61e-7c007f4db321 |
| PRODUCT NDC: | 65649-201 |
| APPLICATION NUMBER: | NDA021881 |