# FESOTERODINE FUMARATE

NDC: 31722-034
Generic name: FESOTERODINE FUMARATE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240109

FDA application: ANDA204792

## Active ingredients

- FESOTERODINE FUMARATE: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-034"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-034
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc532c6c-ff0d-488a-8a92-b1b0f37c944e