# lurasidone hydrochloride

NDC: 68180-673
Generic name: lurasidone hydrochloride
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230220

FDA application: ANDA208031

## Active ingredients

- LURASIDONE HYDROCHLORIDE: 80 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-673"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-673
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74f2429b-71df-47f0-9cb5-98685372a9b8