Package 72854-209-20

{"route": ["ORAL"], "spl_id": "35322ca5-3819-1ec8-e063-6394a90a262f", "openfda": {"upc": ["0363824999364"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "YAN7R5L890"], "rxcui": ["2549034"], "spl_set_id": ["35322238-d498-1a52-e063-6394a90ac9c4"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72854-209-20)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-209-20", "marketing_start_date": "20250501"}], "brand_name": "Mucinex Nightshift Sinus Maximum Strength", "product_id": "72854-209_35322ca5-3819-1ec8-e063-6394a90a262f", "dosage_form": "TABLET, 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": "72854-209", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Nightshift Sinus", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "1.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}