Package 50580-446-01

{"route": ["ORAL"], "spl_id": "3a1abd26-c0a9-8a65-e063-6294a90ab66e", "openfda": {"upc": ["0300450157348"], "unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["247324"], "spl_set_id": ["1a17b24a-8022-4e2f-e063-6294a90af276"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-446-01)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-446-01", "marketing_start_date": "20240826"}], "brand_name": "EXTRA STRENGTH TYLENOL SEVERE COUGH PLUS SORE THROAT DAY", "product_id": "50580-446_3a1abd26-c0a9-8a65-e063-6294a90ab66e", "dosage_form": "TABLET, FILM COATED", "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": "50580-446", "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": "500 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240826", "listing_expiration_date": "20261231"}