Package 67046-1637-3

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1637-3
Digits Only 6704616373
Product NDC 67046-1637
Product ID 67046-1637_4742c86b-0f0d-1222-e063-6394a90a6ab0
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1637-3)

Marketing

Marketing Status
Marketed Since 2025-12-31
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": "4742c86b-0f0d-1222-e063-6394a90a6ab0", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031"], "spl_set_id": ["4742c2fd-303b-da08-e063-6294a90a7621"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1637-3)", "package_ndc": "67046-1637-3", "marketing_start_date": "20251231"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "67046-1637_4742c86b-0f0d-1222-e063-6394a90a6ab0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67046-1637", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA213248", "marketing_category": "ANDA", "marketing_start_date": "20251231", "listing_expiration_date": "20261231"}