Package 37808-556-09

{"route": ["ORAL"], "spl_id": "83db5e30-ceff-4d74-85e5-17bc70273b9c", "openfda": {"upc": ["0041220359912"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["21a4cc76-a7cb-4d11-bd1b-7d5c6a332f2a"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-556-09)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-556-09", "marketing_start_date": "20071217"}, {"sample": false, "description": "80 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-556-31)", "package_ndc": "37808-556-31", "marketing_start_date": "20071217"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "37808-556_83db5e30-ceff-4d74-85e5-17bc70273b9c", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-556", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "brand_name_suffix": "Extra Strength", "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": "20071217", "listing_expiration_date": "20261231"}