# lurasidone hydrochloride

NDC: 0904-7355
Generic name: lurasidone hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230104

FDA application: ANDA212244

## Active ingredients

- LURASIDONE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7355"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7355
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d8b9ba36-fb02-4f52-b0ed-7fdd81d50c4c