Package 51407-833-05

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-833-05
Digits Only 5140783305
Product NDC 51407-833
Product ID 51407-833_4655e19e-554d-0a05-e063-6294a90ab7a9
Description

500 TABLET, FILM COATED in 1 BOTTLE (51407-833-05)

Marketing

Marketing Status
Discontinued 2026-09-30
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": "4655e19e-554d-0a05-e063-6294a90ab7a9", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041"], "spl_set_id": ["08ba1a4c-c193-e0ea-e063-6294a90a52dc"], "manufacturer_name": ["Golden State Medical Supply, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (51407-833-05)", "package_ndc": "51407-833-05", "marketing_end_date": "20260930", "marketing_start_date": "20231023"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "51407-833_4655e19e-554d-0a05-e063-6294a90ab7a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "51407-833", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA208058", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20190904"}