# solifenacin succinate

NDC: 68462-387
Generic name: solifenacin succinate
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190520

FDA application: ANDA209239

## 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:"68462-387"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-387
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=010c0657-c907-477f-8bd7-5d455a5f50eb