Package 16729-348-10

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16729-348-10
Digits Only 1672934810
Product NDC 16729-348
Product ID 16729-348_415fe396-0d31-40a9-e063-6294a90a8462
Description

30 TABLET, FILM COATED in 1 BOTTLE (16729-348-10)

Marketing

Marketing Status
Marketed Since 2023-02-20
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": "415fe396-0d31-40a9-e063-6294a90a8462", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["7e11ec22-63c1-41a6-899c-4fe746f76bd0"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16729-348-10)", "package_ndc": "16729-348-10", "marketing_start_date": "20230220"}], "brand_name": "lurasidone hydrochloride", "product_id": "16729-348_415fe396-0d31-40a9-e063-6294a90a8462", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "16729-348", "generic_name": "lurasidone hydrochloride", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208049", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}