# Fesoterodine fumarate

NDC: 43598-247
Generic name: Fesoterodine fumarate
Labeler / Manufacturer: Dr.Reddy's Laboratories Inc.,
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220610

FDA application: ANDA204975

## 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:"43598-247"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-247
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5c5d2a97-9029-744f-c410-a4bbbe9761a8