Package 70518-4563-0

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4563-0
Digits Only 7051845630
Product NDC 70518-4563
Product ID 70518-4563_4a2897c8-512e-f2ee-e063-6394a90a8f51
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4563-0)

Marketing

Marketing Status
Marketed Since 2026-02-03
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a2897c8-512e-f2ee-e063-6394a90a8f51", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1235247"], "spl_set_id": ["0115b2fa-4c11-4f91-abe7-8293903e066c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4563-0)", "package_ndc": "70518-4563-0", "marketing_start_date": "20260203"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "70518-4563_4a2897c8-512e-f2ee-e063-6394a90a8f51", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4563", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA218174", "marketing_category": "ANDA", "marketing_start_date": "20260203", "listing_expiration_date": "20271231"}