lurasidone hydrochloride
Generic: lurasidone hydrochloride
Labeler: heritage pharma labs inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
lurasidone hydrochloride
Generic Name
lurasidone hydrochloride
Labeler
heritage pharma labs inc. d/b/a avet pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
lurasidone hydrochloride 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
23155-888
Product ID
23155-888_0827fe43-e438-44c3-9962-7491d04b445d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208058
Listing Expiration
2026-12-31
Marketing Start
2023-10-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155888
Hyphenated Format
23155-888
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lurasidone hydrochloride (source: ndc)
Generic Name
lurasidone hydrochloride (source: ndc)
Application Number
ANDA208058 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (23155-888-03)
- 500 TABLET, FILM COATED in 1 BOTTLE (23155-888-05)
- 90 TABLET, FILM COATED in 1 BOTTLE (23155-888-09)
- 60500 TABLET, FILM COATED in 1 CONTAINER (23155-888-18)
Packages (4)
Ingredients (1)
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": "30 TABLET, FILM COATED in 1 BOTTLE (23155-888-03)", "package_ndc": "23155-888-03", "marketing_start_date": "20231019"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (23155-888-05)", "package_ndc": "23155-888-05", "marketing_start_date": "20250820"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (23155-888-09)", "package_ndc": "23155-888-09", "marketing_start_date": "20250820"}, {"sample": false, "description": "60500 TABLET, FILM COATED in 1 CONTAINER (23155-888-18)", "package_ndc": "23155-888-18", "marketing_start_date": "20231019"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "23155-888_0827fe43-e438-44c3-9962-7491d04b445d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "23155-888", "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": "40 mg/1"}], "application_number": "ANDA208058", "marketing_category": "ANDA", "marketing_start_date": "20231019", "listing_expiration_date": "20261231"}