Package 80425-0089-2

{"route": ["ORAL"], "spl_id": "2a9914b1-cac7-a414-e063-6394a90a6f0d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["b33caad1-8d40-16f2-e053-2a95a90a1b2d"], "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": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0089-1)", "package_ndc": "80425-0089-1", "marketing_start_date": "20151230"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0089-2)", "package_ndc": "80425-0089-2", "marketing_start_date": "20151230"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (80425-0089-3)", "package_ndc": "80425-0089-3", "marketing_start_date": "20151230"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0089-4)", "package_ndc": "80425-0089-4", "marketing_start_date": "20151230"}], "brand_name": "Ibuprofen", "product_id": "80425-0089_2a9914b1-cac7-a414-e063-6394a90a6f0d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0089", "generic_name": "Ibuprofen", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20261231"}