Package 65162-882-09

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65162-882-09
Digits Only 6516288209
Product NDC 65162-882
Description

90 TABLET, COATED in 1 BOTTLE (65162-882-09)

Marketing

Marketing Status
Marketed Since 2023-01-02
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cfb63983-dd01-4006-b387-7e8cfec0699d", "openfda": {"upc": ["0365162882032", "0365162880038", "0365162879032", "0365162082036", "0365162881035"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["6ef0b2f9-9356-4f61-a2fa-e7c2c77a5d3a"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (65162-882-03)", "package_ndc": "65162-882-03", "marketing_start_date": "20230102"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (65162-882-09)", "package_ndc": "65162-882-09", "marketing_start_date": "20230102"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (65162-882-50)", "package_ndc": "65162-882-50", "marketing_start_date": "20230102"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "65162-882_cfb63983-dd01-4006-b387-7e8cfec0699d", "dosage_form": "TABLET, COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "65162-882", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA208002", "marketing_category": "ANDA", "marketing_start_date": "20230102", "listing_expiration_date": "20261231"}