# Lurasidone Hydrochloride

NDC: 62332-495
Generic name: Lurasidone Hydrochloride
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230124

FDA application: ANDA213248

## Active ingredients

- LURASIDONE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-495"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-495
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1cc441b3-0a23-4c68-a90e-436030b7daf2