High Outlier
Strength
4 mg/1
Manufacturer
Pfizer Inc.NDC
00069024230
Classification
Brand
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
FESOTERODINE FUMARATEApproval Type
New Drug (NDA)
FDA Application
NDA022030On Market Since
10/31/2008
Related Drugs
Same classification
No related drugs found.