Package 68071-3849-4

{"route": ["ORAL"], "spl_id": "3520dfb1-22ac-c3e8-e063-6294a90af543", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071384949"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["3520deb7-5e45-3d0f-e063-6394a90ab44b"], "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": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-3849-4)", "package_ndc": "68071-3849-4", "marketing_start_date": "20250514"}], "brand_name": "Ibuprofen", "product_id": "68071-3849_3520dfb1-22ac-c3e8-e063-6294a90af543", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-3849", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}