Package 65162-627-10

{"route": ["ORAL"], "spl_id": "b0cfacfd-b823-4d43-93cc-2c30baa39fe5", "openfda": {"upc": ["0365162627503"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["58b802cb-2443-4f5b-9718-7d54c6d50cb4"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (65162-627-01)", "package_ndc": "65162-627-01", "marketing_start_date": "20101115"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (65162-627-10)", "package_ndc": "65162-627-10", "marketing_start_date": "20101115"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (65162-627-11)", "package_ndc": "65162-627-11", "marketing_start_date": "20101115"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (65162-627-50)", "package_ndc": "65162-627-50", "marketing_start_date": "20101115"}], "brand_name": "Tramadol Hydrochloride", "product_id": "65162-627_b0cfacfd-b823-4d43-93cc-2c30baa39fe5", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "65162-627", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA076003", "marketing_category": "ANDA", "marketing_start_date": "20101115", "listing_expiration_date": "20261231"}