# lurasidone hydrochloride

NDC: 67877-641
Generic name: lurasidone hydrochloride
Labeler / Manufacturer: Ascend Laboratories, LLC
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: 80 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-641"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-641
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36b6bacd-ac11-493b-a8a4-8dad448ed9d5