# LURASIDONE HYDROCHLORIDE

NDC: 65862-957
Generic name: LURASIDONE HYDROCHLORIDE
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230310

FDA application: ANDA208045

## Active ingredients

- LURASIDONE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-957"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-957
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b3e9cc86-0c5c-444f-ab57-f4d1a6865035