Package 70518-4241-0

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4241-0
Digits Only 7051842410
Product NDC 70518-4241
Product ID 70518-4241_40077a1f-b3ad-07e2-e063-6394a90a6d2a
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4241-0)

Marketing

Marketing Status
Marketed Since 2024-12-16
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": "40077a1f-b3ad-07e2-e063-6394a90a6d2a", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1235247"], "spl_set_id": ["a97b59db-29e8-4b00-9d35-56b47335ee25"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4241-0)", "package_ndc": "70518-4241-0", "marketing_start_date": "20241216"}], "brand_name": "Lurasidone hydrochloride", "product_id": "70518-4241_40077a1f-b3ad-07e2-e063-6394a90a6d2a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4241", "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": "ANDA208047", "marketing_category": "ANDA", "marketing_start_date": "20241216", "listing_expiration_date": "20261231"}