Package 58602-760-73

{"route": ["ORAL"], "spl_id": "0b448607-8f69-f9b8-e063-6394a90ae841", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "spl_set_id": ["3ba51b52-7ae6-4335-b178-1b7b6ef36227"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-760-14)  / 50 TABLET in 1 BOTTLE", "package_ndc": "58602-760-14", "marketing_start_date": "20210105"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-760-73)  / 20 TABLET in 1 BOTTLE", "package_ndc": "58602-760-73", "marketing_start_date": "20210105"}], "brand_name": "Acetaminophen and Diphenhydramine hydrochloride", "product_id": "58602-760_0b448607-8f69-f9b8-e063-6394a90ae841", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "58602-760", "generic_name": "Acetaminophen and Diphenhydramine hydrochloride", "labeler_name": "Aurohealth LLC", "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": "20210105", "listing_expiration_date": "20261231"}