# Lurasidone Hydrochloride

NDC: 53746-082
Generic name: Lurasidone Hydrochloride
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20240705

FDA application: ANDA208002

## Active ingredients

- LURASIDONE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53746-082"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53746-082
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=84648adf-b3c6-476e-8d11-2a9d7c5eb550