Package 70518-4491-0

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4491-0
Digits Only 7051844910
Product NDC 70518-4491
Product ID 70518-4491_407c6e44-e2fc-7523-e063-6394a90af312
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4491-0)

Marketing

Marketing Status
Marketed Since 2025-10-04
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": "407c6e44-e2fc-7523-e063-6394a90af312", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031"], "spl_set_id": ["b94e9272-ed67-4af8-827a-4b8cc3b168a1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4491-0)", "package_ndc": "70518-4491-0", "marketing_start_date": "20251004"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "70518-4491_407c6e44-e2fc-7523-e063-6394a90af312", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4491", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA218174", "marketing_category": "ANDA", "marketing_start_date": "20251004", "listing_expiration_date": "20261231"}