Package 68788-8322-4

{"route": ["ORAL"], "spl_id": "1618f962-f180-47ed-a7a2-37c5597f9923", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197803"], "spl_set_id": ["65f1ddd2-7b55-4cce-bed6-07e9cf29e3ae"], "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": "473 mL in 1 BOTTLE (68788-8322-4)", "package_ndc": "68788-8322-4", "marketing_start_date": "20230123"}], "brand_name": "Ibuprofen", "product_id": "68788-8322_1618f962-f180-47ed-a7a2-37c5597f9923", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8322", "generic_name": "Ibuprofen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "100 mg/5mL"}], "application_number": "ANDA076925", "marketing_category": "ANDA", "marketing_start_date": "20230123", "listing_expiration_date": "20261231"}