# Lurasidone Hydrochloride

NDC: 13668-737
Generic name: Lurasidone Hydrochloride
Labeler / Manufacturer: Torrent Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260302

FDA application: ANDA208055

## Active ingredients

- LURASIDONE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13668-737"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13668-737
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9cb5e275-1029-407a-8c93-ec5cde2d323b