{ "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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ORAL SOLUTION", "KALI MURIATICUM KIT REFILL", "POKONZA", "D-125" ], "generic_name": [ "POTASSIUM CHLORIDE", "POTASSIUM CHLORIDE EXTENDED-RELEASE", "POTASSIUM CHLORIDE, DEXTROSE MONOHYDRATE", "POTASSIUM CHLORIDE ORAL" ], "manufacturer_name": [ "Zydus Lifesciences Limited", "Hyland's Inc.", "Zydus Pharmaceuticals (USA) Inc.", "Camber Pharmaceuticals, Inc.", "Epic Pharma, LLC", "DelCorean, LLC", "PAI Holdings, LLC dba PAI Pharma", "Actavis Pharma, Inc.", "Solco Healthcare LLC", "Northstar Rx LLC", "Granules India Ltd", "Lupin Pharmaceuticals,Inc.", "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "Hospira, Inc.", "Sun Pharmaceutical Industries, Inc.", "Boiron", "Macleods Pharmaceuticals Limited", "Granules Pharmaceuticals Inc.", "Amneal Pharmaceuticals NY LLC", "Genus Lifesciences Inc.", "Guardian Drug Company", "Fresenius Kabi USA, LLC", "Aurobindo Pharma Limited", "BPI Labs LLC", "Upsher-Smith Laboratories, LLC", "Adare Pharmaceuticals Inc", "Kesin Pharma Corporation", 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"Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]" ], "pharm_class_moa": [ "Osmotic Activity [MoA]" ] } }, { "drugcharacterization": "2", "medicinalproduct": "ATORVASTATIN", "drugstructuredosagenumb": "10", "drugstructuredosageunit": "003", "drugdosageform": "UNSPECIFIED", "drugadministrationroute": "048", "activesubstance": { "activesubstancename": "ATORVASTATIN" } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 20131001" } } } ] }