# fesoterodine fumarate

NDC: 68382-479
Generic name: fesoterodine fumarate
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20171207

FDA application: ANDA204946

## Active ingredients

- FESOTERODINE FUMARATE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-479"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-479
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8c68e918-b47b-466d-80bc-4f521aa74607