Package 68788-8319-7

{"route": ["ORAL"], "spl_id": "f9e16ed0-28fd-4b93-a4b4-1c99eb9da6d5", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["25d9f5fc-4d95-4018-add8-ba696b6079b2"], "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": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8319-1)", "package_ndc": "68788-8319-1", "marketing_start_date": "20221223"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8319-2)", "package_ndc": "68788-8319-2", "marketing_start_date": "20221223"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8319-3)", "package_ndc": "68788-8319-3", "marketing_start_date": "20221223"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-8319-4)", "package_ndc": "68788-8319-4", "marketing_start_date": "20221223"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (68788-8319-5)", "package_ndc": "68788-8319-5", "marketing_start_date": "20221223"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8319-6)", "package_ndc": "68788-8319-6", "marketing_start_date": "20221223"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68788-8319-7)", "package_ndc": "68788-8319-7", "marketing_start_date": "20221223"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-8319-8)", "package_ndc": "68788-8319-8", "marketing_start_date": "20221223"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8319-9)", "package_ndc": "68788-8319-9", "marketing_start_date": "20221223"}], "brand_name": "Ibuprofen", "product_id": "68788-8319_f9e16ed0-28fd-4b93-a4b4-1c99eb9da6d5", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8319", "generic_name": "Ibuprofen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA213794", "marketing_category": "ANDA", "marketing_start_date": "20221223", "listing_expiration_date": "20261231"}