Package 70518-4117-0

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4117-0
Digits Only 7051841170
Product NDC 70518-4117
Product ID 70518-4117_3d310ff4-f668-b9d5-e063-6394a90af777
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4117-0)

Marketing

Marketing Status
Marketed Since 2024-06-27
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3d310ff4-f668-b9d5-e063-6394a90af777", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031"], "spl_set_id": ["672d22f6-fad5-49db-9206-f924d02af181"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4117-0)", "package_ndc": "70518-4117-0", "marketing_start_date": "20240627"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4117-1)", "package_ndc": "70518-4117-1", "marketing_start_date": "20250823"}], "brand_name": "Lurasidone hydrochloride", "product_id": "70518-4117_3d310ff4-f668-b9d5-e063-6394a90af777", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4117", "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": "ANDA208047", "marketing_category": "ANDA", "marketing_start_date": "20240627", "listing_expiration_date": "20261231"}