{"effective_time":"20230607","how_supplied":["HOW SUPPLIED Product: 53002-3011 NDC: 53002-3011-1 10 TABLET, FILM COATED in a BOTTLE NDC: 53002-3011-2 15 TABLET, FILM COATED in a BOTTLE NDC: 53002-3011-4 30 TABLET, FILM COATED in a BOTTLE NDC: 53002-3011-5 50 TABLET, FILM COATED in a BOTTLE"],"id":"e02a2964-1671-4427-84ac-80adf6c0e05c","openfda":{},"package_label_principal_display_panel":["Ibuprofen 600mg Tablets, USP Label Image"],"set_id":"2913f3f3-6998-4f24-ae35-2ba834f7ddd2","spl_medguide":["ibuprofen tablets 400 mg - 600 mg- 800 mg medguide MEDGUIDE IBUPROFEN TABLETS"],"spl_product_data_elements":["IBUPROFEN IBUPROFEN SILICON DIOXIDE CROSCARMELLOSE SODIUM MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL, UNSPECIFIED POLYVINYL ALCOHOL, UNSPECIFIED STARCH, CORN TALC TITANIUM DIOXIDE IBUPROFEN IBUPROFEN 122"],"version":"3"}