# vilazodone hydrochloride

NDC: 68788-8734
Generic name: vilazodone hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240916

FDA application: ANDA208228

## Active ingredients

- VILAZODONE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8734"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8734
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=061efdcc-40ea-4647-8cc8-01cd1ccca68b