# Solifenacin succinate

NDC: 0591-3796
Generic name: solifenacin succinate
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200409

FDA application: ANDA202551

## Active ingredients

- SOLIFENACIN SUCCINATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0591-3796"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0591-3796
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02e2aa54-1ed8-445a-a082-ac2c64b339fe