Package 50580-140-08

{"route": ["ORAL"], "spl_id": "2e9540e4-bd1e-9370-e063-6294a90affcb", "openfda": {"upc": ["0300450565082"], "unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["1359455"], "spl_set_id": ["2e9540e4-bd1d-9370-e063-6294a90affcb"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (50580-140-08)", "package_ndc": "50580-140-08", "marketing_start_date": "20250606"}], "brand_name": "Extra Strength TYLENOL Severe Cough Plus Sore Throat Day", "product_id": "50580-140_2e9540e4-bd1e-9370-e063-6294a90affcb", "dosage_form": "LIQUID", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "50580-140", "generic_name": "acetaminophen and dextromethorphan hydrobromide", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength TYLENOL Severe Cough Plus Sore Throat Day", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250606", "listing_expiration_date": "20261231"}