# Solifenacin succinate

NDC: 72303-0832
Generic name: solifenacin succinate
Labeler / Manufacturer: HEC Pharm USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260701

FDA application: ANDA213346

## 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:"72303-0832"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72303-0832
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56026679-4002-a6c6-e063-6294a90a7b55