Package 13668-509-30

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13668-509-30
Digits Only 1366850930
Product NDC 13668-509
Product ID 13668-509_dba1819d-0cd5-4522-9666-5155aa9e0085
Description

30 TABLET, FILM COATED in 1 BOTTLE (13668-509-30)

Marketing

Marketing Status
Marketed Since 2023-02-17
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": "dba1819d-0cd5-4522-9666-5155aa9e0085", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1431235"], "spl_set_id": ["a101e62e-dd1f-4add-8393-ba6d54adce06"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13668-509-30)", "package_ndc": "13668-509-30", "marketing_start_date": "20230217"}], "brand_name": "Lurasidone hydrochloride", "product_id": "13668-509_dba1819d-0cd5-4522-9666-5155aa9e0085", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "13668-509", "generic_name": "Lurasidone hydrochloride", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208047", "marketing_category": "ANDA", "marketing_start_date": "20230217", "listing_expiration_date": "20261231"}