Package 72189-324-60

{"route": ["ORAL"], "spl_id": "2c3d44ba-dd1c-19fc-e063-6394a90a15f9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805"], "spl_set_id": ["d88d0544-57a7-4a82-e053-2a95a90a1945"], "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": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-324-30)", "package_ndc": "72189-324-30", "marketing_start_date": "20220221"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-324-60)", "package_ndc": "72189-324-60", "marketing_start_date": "20220221"}], "brand_name": "IBUPROFEN", "product_id": "72189-324_2c3d44ba-dd1c-19fc-e063-6394a90a15f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72189-324", "generic_name": "IBUPROFEN", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20220221", "listing_expiration_date": "20261231"}