Package 51407-837-05

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-837-05
Digits Only 5140783705
Product NDC 51407-837
Product ID 51407-837_4423d3dd-2de0-ff56-e063-6294a90ab1e3
Description

500 TABLET, FILM COATED in 1 BOTTLE (51407-837-05)

Marketing

Marketing Status
Marketed Since 2024-02-03
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": "4423d3dd-2de0-ff56-e063-6294a90ab1e3", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1235247", "1297278", "1431235"], "spl_set_id": ["1989d512-e568-468f-e063-6294a90a5c22"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (51407-837-05)", "package_ndc": "51407-837-05", "marketing_start_date": "20240203"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "51407-837_4423d3dd-2de0-ff56-e063-6294a90ab1e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "51407-837", "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": "60 mg/1"}], "application_number": "ANDA208058", "marketing_category": "ANDA", "marketing_start_date": "20190904", "listing_expiration_date": "20261231"}