# TOLTERODINE TARTRATE

NDC: 0904-6593
Generic name: TOLTERODINE
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20150811
Marketing ended: 20260731
FDA application: ANDA203016

## Active ingredients

- TOLTERODINE TARTRATE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-6593"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-6593
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da9423b5-00ab-46fc-8959-3db3c0a0bc6d