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fesoterodine fumarate

NDC 68382-480 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204946
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsFESOTERODINE FUMARATE (8 mg/1)
Marketing started20171207
Package count3

External sources

Source: openFDA. Public-domain (CC0).