Package 23155-891-03

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 23155-891-03
Digits Only 2315589103
Product NDC 23155-891
Description

30 TABLET, FILM COATED in 1 BOTTLE (23155-891-03)

Marketing

Marketing Status
Marketed Since 2025-08-20
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0827fe43-e438-44c3-9962-7491d04b445d", "openfda": {"upc": ["0323155888034", "0323155887099", "0323155891034", "0323155887037", "0323155890099", "0323155889093", "0323155888096", "0323155890037", "0323155889031"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["083a1a52-5a13-4e28-8ef2-127ac4ce5b2d"], "manufacturer_name": ["Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (23155-891-01)", "package_ndc": "23155-891-01", "marketing_start_date": "20250820"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (23155-891-03)", "package_ndc": "23155-891-03", "marketing_start_date": "20250820"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (23155-891-05)", "package_ndc": "23155-891-05", "marketing_start_date": "20250820"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (23155-891-10)", "package_ndc": "23155-891-10", "marketing_start_date": "20250820"}, {"sample": false, "description": "20000 TABLET, FILM COATED in 1 CONTAINER (23155-891-18)", "package_ndc": "23155-891-18", "marketing_start_date": "20231019"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "23155-891_0827fe43-e438-44c3-9962-7491d04b445d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "23155-891", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA208058", "marketing_category": "ANDA", "marketing_start_date": "20231019", "listing_expiration_date": "20261231"}