Package 70518-4259-0

{"route": ["ORAL"], "spl_id": "4008c27b-717f-9f90-e063-6294a90a725f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["404df13d-4ada-4324-9eed-e21f5d5043a4"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4259-0)", "package_ndc": "70518-4259-0", "marketing_start_date": "20250122"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4259-1)", "package_ndc": "70518-4259-1", "marketing_start_date": "20250122"}], "brand_name": "Ibuprofen", "product_id": "70518-4259_4008c27b-717f-9f90-e063-6294a90a725f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-4259", "generic_name": "Ibuprofen", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20250122", "listing_expiration_date": "20261231"}