Package 67046-1654-3

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1654-3
Digits Only 6704616543
Product NDC 67046-1654
Product ID 67046-1654_4973bdb9-ab5c-58eb-e063-6294a90a883e
Description

30 TABLET in 1 BLISTER PACK (67046-1654-3)

Marketing

Marketing Status
Marketed Since 2026-01-28
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": "4973bdb9-ab5c-58eb-e063-6294a90a883e", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1431235"], "spl_set_id": ["4973beed-b75b-c370-e063-6394a90a26e5"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1654-3)", "package_ndc": "67046-1654-3", "marketing_start_date": "20260128"}], "brand_name": "LURASIDONE HYDROCHLORIDE", "product_id": "67046-1654_4973bdb9-ab5c-58eb-e063-6294a90a883e", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67046-1654", "generic_name": "LURASIDONE HYDROCHLORIDE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LURASIDONE HYDROCHLORIDE", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208045", "marketing_category": "ANDA", "marketing_start_date": "20260128", "listing_expiration_date": "20271231"}