Toviaz (U.S. Pharmaceuticals)
Welcome to the PulseAid listing for the Toviaz drug offered from U.S. Pharmaceuticals. 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: | U.S. Pharmaceuticals |
| NON-PROPRIETARY NAME: | fesoterodine fumarate |
| SUBSTANCE NAME: | FESOTERODINE FUMARATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2008-10-31 |
| END MARKETING DATE: | 0000-00-00 |
Toviaz HUMAN PRESCRIPTION DRUG Details:
| Item Description | Toviaz from U.S. Pharmaceuticals |
| LABELER NAME: | U.S. Pharmaceuticals |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 8(mg/1) |
| START MARKETING DATE: | 2008-10-31 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63539-183_47f19c39-9fd2-4471-9d91-08da92d4fb68 |
| PRODUCT NDC: | 63539-183 |
| APPLICATION NUMBER: | NDA022030 |
Other FESOTERODINE FUMARATE Pharmaceutical Manufacturers / Labelers:
