# Detrol

NDC: 58151-099
Generic name: tolterodine tartrate
Labeler / Manufacturer: Viatris Specialty LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240801
Marketing ended: 20270131
FDA application: NDA020771

## Active ingredients

- TOLTERODINE TARTRATE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58151-099"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58151-099
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=41eb00d2-64e3-4ec9-8732-4bfc81b04180