Package 50580-598-02

{"route": ["ORAL"], "spl_id": "21acf19d-d051-97ca-e063-6294a90a5e41", "openfda": {"unii": ["362O9ITL9D", "04JA59TNSJ"], "rxcui": ["1046378"], "spl_set_id": ["e608d214-cc46-4a24-ac85-1040e36e7403"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-598-02)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-598-02", "marketing_start_date": "20190508"}], "brand_name": "TYLENOL SINUS PLUS HEADACHE DAY", "product_id": "50580-598_21acf19d-d051-97ca-e063-6294a90a5e41", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "50580-598", "generic_name": "Acetaminophen and Phenylephrine hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL SINUS PLUS HEADACHE", "brand_name_suffix": "DAY", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150715", "listing_expiration_date": "20261231"}