Strength
4 mg/1
Manufacturer
Zydus Pharmaceuticals (USA) Inc.NDC
68382047906
Classification
Generic
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
FESOTERODINE FUMARATEApproval Type
Generic (ANDA)
FDA Application
ANDA204946On Market Since
12/7/2017
Related Drugs
Same classification
No related drugs found.