Package 63868-210-20

{"route": ["ORAL"], "spl_id": "c2a91066-4981-42c6-9a60-0841c1c3d2af", "openfda": {"upc": ["0635515993686"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["bbc704e5-79f6-4c72-846b-cc30c5c43cb4"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-210-20)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-210-20", "marketing_end_date": "20261231", "marketing_start_date": "20071217"}], "brand_name": "Acetaminophen PM Extra Strength", "product_id": "63868-210_c2a91066-4981-42c6-9a60-0841c1c3d2af", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63868-210", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "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": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20071217"}