Package 72205-208-90

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72205-208-90
Digits Only 7220520890
Product NDC 72205-208
Product ID 72205-208_8f42d8c8-cccf-49e3-9bad-e9a45d8d7896
Description

90 TABLET, FILM COATED in 1 BOTTLE (72205-208-90)

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": "8f42d8c8-cccf-49e3-9bad-e9a45d8d7896", "openfda": {"upc": ["0372205208308", "0372205209053", "0372205209909", "0372205210905", "0372205209305", "0372205210301", "0372205211902", "0372205207059", "0372205211308", "0372205210059", "0372205211056", "0372205208056", "0372205207301", "0372205208902", "0372205207905"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["4f969224-a9f0-4089-84d6-a15664ea7bfe"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72205-208-05)", "package_ndc": "72205-208-05", "marketing_start_date": "20230220"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-208-30)", "package_ndc": "72205-208-30", "marketing_start_date": "20230220"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72205-208-90)", "package_ndc": "72205-208-90", "marketing_start_date": "20230220"}], "brand_name": "lurasidone hydrochloride", "product_id": "72205-208_8f42d8c8-cccf-49e3-9bad-e9a45d8d7896", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72205-208", "generic_name": "lurasidone hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208037", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20261231"}