Package 70512-794-90

{"route": ["ORAL"], "spl_id": "3a6156f7-9a9c-01d8-e063-6394a90aa500", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0370512794903"], "unii": ["WK2XYI10QM"], "rxcui": ["197804"], "spl_set_id": ["44fb0842-c34e-477e-96df-350cd5d6800e"], "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": ["SOLA Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70512-794-90)", "package_ndc": "70512-794-90", "marketing_start_date": "20250214"}], "brand_name": "Ibuprofen", "product_id": "70512-794_3a6156f7-9a9c-01d8-e063-6394a90aa500", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70512-794", "generic_name": "ibuprofen", "labeler_name": "SOLA Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "300 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20250214", "listing_expiration_date": "20261231"}