Package 85509-2396-6

{"route": ["ORAL"], "spl_id": "3b51bdea-0879-d416-e063-6394a90a84b4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["3b17587e-b609-42a9-e063-6294a90ab1f8"], "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": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85509-2396-3)", "package_ndc": "85509-2396-3", "marketing_start_date": "20250730"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85509-2396-6)", "package_ndc": "85509-2396-6", "marketing_start_date": "20250730"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85509-2396-9)", "package_ndc": "85509-2396-9", "marketing_start_date": "20250730"}], "brand_name": "Ibuprofen", "product_id": "85509-2396_3b51bdea-0879-d416-e063-6394a90a84b4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "85509-2396", "generic_name": "Ibuprofen", "labeler_name": "PHOENIX RX LLC", "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": "20240523", "listing_expiration_date": "20261231"}