Package 68788-8354-5

{"route": ["ORAL"], "spl_id": "e8f4cfea-ec98-4348-bb24-55585ed25e80", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["13fd4401-1821-4f2b-a44e-96aa2fa75b5c"], "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 (68788-8354-1)", "package_ndc": "68788-8354-1", "marketing_start_date": "20230210"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8354-2)", "package_ndc": "68788-8354-2", "marketing_start_date": "20230210"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8354-3)", "package_ndc": "68788-8354-3", "marketing_start_date": "20230210"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-8354-4)", "package_ndc": "68788-8354-4", "marketing_start_date": "20230210"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (68788-8354-5)", "package_ndc": "68788-8354-5", "marketing_start_date": "20230210"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8354-6)", "package_ndc": "68788-8354-6", "marketing_start_date": "20230210"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68788-8354-7)", "package_ndc": "68788-8354-7", "marketing_start_date": "20230210"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-8354-8)", "package_ndc": "68788-8354-8", "marketing_start_date": "20230210"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8354-9)", "package_ndc": "68788-8354-9", "marketing_start_date": "20230210"}], "brand_name": "Ibuprofen", "product_id": "68788-8354_e8f4cfea-ec98-4348-bb24-55585ed25e80", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8354", "generic_name": "Ibuprofen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA213794", "marketing_category": "ANDA", "marketing_start_date": "20230210", "listing_expiration_date": "20261231"}