Package 83324-178-44

{"route": ["ORAL"], "spl_id": "23994b21-cbbf-5a34-e063-6394a90acfdf", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["23994b21-cbc2-5a34-e063-6394a90acfdf"], "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": ["CHAIN DRUG MARKETING ASSOCIATION INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83324-178-44)  / 144 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "83324-178-44", "marketing_start_date": "20241003"}], "brand_name": "dual action pain reliever", "product_id": "83324-178_23994b21-cbbf-5a34-e063-6394a90acfdf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "83324-178", "generic_name": "Acetaminophen and Ibuprofen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dual action pain reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA216999", "marketing_category": "ANDA", "marketing_start_date": "20241003", "listing_expiration_date": "20261231"}