Package 50228-424-60

Brand: ranolazine

Generic: ranolazine
NDC Package

Package Facts

Identity

Package NDC 50228-424-60
Digits Only 5022842460
Product NDC 50228-424
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (50228-424-60)

Marketing

Marketing Status
Marketed Since 2019-06-04
Brand ranolazine
Generic ranolazine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a0ac71c-e53c-5ff9-e063-6394a90a4807", "openfda": {"nui": ["N0000175427", "N0000190114", "N0000185503", "N0000182137", "N0000187061"], "upc": ["0350228424608", "0350228424301", "0350228423304", "0350228423601"], "unii": ["A6IEZ5M406"], "rxcui": ["616749", "728231"], "spl_set_id": ["71d50258-75b7-4801-b0f4-c34fe883d57d"], "pharm_class_epc": ["Anti-anginal [EPC]"], "pharm_class_moa": ["Cytochrome P450 3A Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]", "Organic Cation Transporter 2 Inhibitors [MoA]"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (50228-424-05)", "package_ndc": "50228-424-05", "marketing_start_date": "20190604"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (50228-424-30)", "package_ndc": "50228-424-30", "marketing_start_date": "20190604"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (50228-424-60)", "package_ndc": "50228-424-60", "marketing_start_date": "20190604"}], "brand_name": "RANOLAZINE", "product_id": "50228-424_2a0ac71c-e53c-5ff9-e063-6394a90a4807", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-anginal [EPC]", "Cytochrome P450 2D6 Inhibitors [MoA]", "Cytochrome P450 3A Inhibitors [MoA]", "Organic Cation Transporter 2 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "50228-424", "generic_name": "RANOLAZINE", "labeler_name": "ScieGen Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RANOLAZINE", "active_ingredients": [{"name": "RANOLAZINE", "strength": "1000 mg/1"}], "application_number": "ANDA211829", "marketing_category": "ANDA", "marketing_start_date": "20190604", "listing_expiration_date": "20261231"}