Package 30142-193-14

{"route": ["ORAL"], "spl_id": "539e230b-aef0-4660-915d-b03b90d647d0", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["b9b86755-63ad-e25a-e053-2995a90ad747"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-193-14)  / 50 TABLET in 1 BOTTLE", "package_ndc": "30142-193-14", "marketing_start_date": "20210306"}], "brand_name": "Acetaminophen and Diphenhydramine hydrochloride", "product_id": "30142-193_539e230b-aef0-4660-915d-b03b90d647d0", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "30142-193", "generic_name": "Acetaminophen and Diphenhydramine hydrochloride", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen and Diphenhydramine hydrochloride", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210306", "listing_expiration_date": "20261231"}