Package 70264-042-01

{"route": ["ORAL"], "spl_id": "43c90d03-e359-6ce4-e063-6394a90a1da2", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["cd3060a5-3b90-42e4-89cd-3b620859045f"], "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": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 CARTON (70264-042-01)  / 2 TABLET, COATED in 1 POUCH", "package_ndc": "70264-042-01", "marketing_start_date": "20241101"}], "brand_name": "Ibuprofen 200 mg", "product_id": "70264-042_43c90d03-e359-6ce4-e063-6394a90a1da2", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70264-042", "generic_name": "Ibuprofen", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen 200 mg", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}