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 |