Package 79903-267-80

{"route": ["ORAL"], "spl_id": "d57e57bb-b700-4f99-9e22-1e887bd85515", "openfda": {"upc": ["0194346263585"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["16d5786c-2346-f970-e063-6394a90a0a8c"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET in 1 BOTTLE (79903-267-80)", "package_ndc": "79903-267-80", "marketing_start_date": "20240628"}], "brand_name": "Acetaminophen and Diphenhydramine hydrochloride", "product_id": "79903-267_d57e57bb-b700-4f99-9e22-1e887bd85515", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "79903-267", "generic_name": "Acetaminophen and Diphenhydramine hydrochloride", "labeler_name": "WALMART INC.", "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": "20240628", "listing_expiration_date": "20261231"}