Package 41163-228-50

{"route": ["ORAL"], "spl_id": "83565dcc-a930-4bd8-8cae-0693325b7559", "openfda": {"upc": ["0041163265394"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["24173e77-92ec-4a87-a471-d6867837c180"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (41163-228-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41163-228-50", "marketing_start_date": "20140829"}], "brand_name": "Acetaminophen PM Extra Strength", "product_id": "41163-228_83565dcc-a930-4bd8-8cae-0693325b7559", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "41163-228", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140829", "listing_expiration_date": "20261231"}