{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. 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"ALENDRONATE" ], "generic_name": [ "ALENDRONATE SODIUM", "ALENDRONATE SODIUM TABLET" ], "manufacturer_name": [ "Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.", "Marlex Pharmaceuticals, Inc." ], "product_ndc": [ "60723-205", "60723-207", "10135-718", "10135-719" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "ORAL" ], "substance_name": [ "ALENDRONATE SODIUM" ], "rxcui": [ "904396", "904431" ], "spl_id": [ "460d461d-4807-2ed0-e063-6394a90aad4a", "3e74abef-2742-2bbe-e063-6394a90a12cd" ], "spl_set_id": [ "a24fd39c-34a7-4de2-9439-781e612189ca", "b63421af-ec03-1de7-e053-2a95a90abec6" ], "package_ndc": [ "60723-205-31", "60723-205-32", "60723-205-33", "60723-207-31", "60723-207-32", "60723-207-33", "10135-718-44", "10135-718-12", "10135-719-44", "10135-719-12", "10135-719-20" ], "unii": [ "2UY4M2U3RA" ] } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 20150113" } } } ] }