Package 52817-196-00

{"route": ["ORAL"], "spl_id": "bb37b29d-c827-d710-e053-2995a90acf1d", "openfda": {"upc": ["0352817196101", "0352817196002", "0352817195005", "0352817196507", "0352817195500", "0352817195104"], "unii": ["9N7R477WCK"], "rxcui": ["835603", "2179635"], "spl_set_id": ["61fb5ba7-6896-4ee4-83de-caee69b06a8e"], "manufacturer_name": ["TRUPHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (52817-196-00)", "package_ndc": "52817-196-00", "marketing_start_date": "20200224"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (52817-196-10)", "package_ndc": "52817-196-10", "marketing_start_date": "20200224"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (52817-196-50)", "package_ndc": "52817-196-50", "marketing_start_date": "20200224"}], "brand_name": "Tramadol Hydrochloride", "product_id": "52817-196_bb37b29d-c827-d710-e053-2995a90acf1d", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "52817-196", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "TRUPHARMA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA208708", "marketing_category": "ANDA", "marketing_start_date": "20200224", "listing_expiration_date": "20261231"}