# Lurasidone hydrochloride

NDC: 70771-1735
Generic name: Lurasidone hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20230201

FDA application: ANDA208052

## Active ingredients

- LURASIDONE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1735"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1735
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f5f8228-1304-4981-8577-029136627260