Package 70518-4427-0

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4427-0
Digits Only 7051844270
Product NDC 70518-4427
Product ID 70518-4427_4041479b-b6e5-6ca7-e063-6294a90a371f
Description

30 TABLET in 1 BLISTER PACK (70518-4427-0)

Marketing

Marketing Status
Marketed Since 2025-08-06
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": "4041479b-b6e5-6ca7-e063-6294a90a371f", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031"], "spl_set_id": ["5dc04e98-e41c-40cb-9037-d29084c9bf6d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4427-0)", "package_ndc": "70518-4427-0", "marketing_start_date": "20250806"}], "brand_name": "lurasidone hydrochloride", "product_id": "70518-4427_4041479b-b6e5-6ca7-e063-6294a90a371f", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4427", "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": "ANDA208031", "marketing_category": "ANDA", "marketing_start_date": "20250806", "listing_expiration_date": "20261231"}