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Fesoterodine fumarate

NDC 43598-247 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDr.Reddy's Laboratories Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA204975
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFESOTERODINE FUMARATE (4 mg/1)
Marketing started20220610
Package count2

External sources

Source: openFDA. Public-domain (CC0).