Home
>
National Drug Code (NDC)
>
Toviaz
Toviaz - 63539-242-03 - (FESOTERODINE FUMARATE)
Drug Information of Toviaz
| Product NDC: | 63539-242 |
| Proprietary Name: | Toviaz |
| Non Proprietary Name: | FESOTERODINE FUMARATE |
| Active Ingredient(s): | 4 mg/1 & nbsp; FESOTERODINE FUMARATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Toviaz
| Product NDC: | 63539-242 |
| Labeler Name: | U.S. Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022030 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081031 |
Package Information of Toviaz
| Package NDC: | 63539-242-03 |
| Package Description: | 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63539-242-03) |
NDC Information of Toviaz
| NDC Code | 63539-242-03 |
| Proprietary Name | Toviaz |
| Package Description | 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63539-242-03) |
| Product NDC | 63539-242 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FESOTERODINE FUMARATE |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20081031 |
| Marketing Category Name | NDA |
| Labeler Name | U.S. Pharmaceuticals |
| Substance Name | FESOTERODINE FUMARATE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
