Package 33342-423-07

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 33342-423-07
Digits Only 3334242307
Product NDC 33342-423
Product ID 33342-423_f4eb6157-0321-467a-a06b-69c2970eda71
Description

30 TABLET, FILM COATED in 1 BOTTLE (33342-423-07)

Marketing

Marketing Status
Marketed Since 2023-06-09
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

lurasidone hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f4eb6157-0321-467a-a06b-69c2970eda71", "openfda": {"upc": ["0333342420107", "0333342423108", "0333342419101", "0333342420077", "0333342419071", "0333342423078", "0333342422101"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["2b07a830-93ba-427a-95fc-5138a6309f1e"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (33342-423-07)", "package_ndc": "33342-423-07", "marketing_start_date": "20230609"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-423-10)", "package_ndc": "33342-423-10", "marketing_start_date": "20230609"}], "brand_name": "lurasidone hydrochloride", "product_id": "33342-423_f4eb6157-0321-467a-a06b-69c2970eda71", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "33342-423", "generic_name": "lurasidone hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA212124", "marketing_category": "ANDA", "marketing_start_date": "20230609", "listing_expiration_date": "20261231"}