# Lurasidone Hydrochloride

NDC: 23155-889
Generic name: Lurasidone Hydrochloride
Labeler / Manufacturer: Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20231019

FDA application: ANDA208058

## 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:"23155-889"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-889
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=083a1a52-5a13-4e28-8ef2-127ac4ce5b2d