Package 68180-673-06

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-673-06
Digits Only 6818067306
Product NDC 68180-673
Product ID 68180-673_8d77b0dd-8cc2-44da-afed-1e5cb75bed99
Description

30 TABLET in 1 BOTTLE (68180-673-06)

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": "8d77b0dd-8cc2-44da-afed-1e5cb75bed99", "openfda": {"upc": ["0368180671060", "0368180673064", "0368180672067", "0368180670063", "0368180674061"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["74f2429b-71df-47f0-9cb5-98685372a9b8"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68180-673-06)", "package_ndc": "68180-673-06", "marketing_start_date": "20230220"}], "brand_name": "lurasidone hydrochloride", "product_id": "68180-673_8d77b0dd-8cc2-44da-afed-1e5cb75bed99", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68180-673", "generic_name": "lurasidone hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA208031", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}