# Solifenacin Succinate

NDC: 65862-879
Generic name: Solifenacin Succinate
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221227

FDA application: ANDA206817

## 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:"65862-879"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-879
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92b37f2d-b1cf-49e6-a13b-0ead92c0604c