{"@type": "dcat:Dataset", "accessLevel": "public", "accrualPeriodicity": "R/P1Y", "bureauCode": ["009:10"], "contactPoint": {"@type": "vcard:Contact", "fn": "Division of Drug Information", "hasEmail": "mailto:druginfo@fda.hhs.gov"}, "description": "Potassium Chloride is an injectable prescription drug used to treat or prevent low potassium levels in the blood. It comes as a 2 mEq/mL solution in 10 mL glass vials, administered intravenously by healthcare professionals. Manufactured by Nexus Pharmaceuticals LLC under ANDA217704. This information was generated using AI and is provided for informational and research purposes only.", "distribution": [{"@type": "dcat:Distribution", "description": "\n        Access the FDA dataset for Potassium chloride \u2014 ANDA 209688 submitted by Mylan Institutional LLC\n    ", "downloadURL": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=209688", "mediaType": "text/html", "title": "Potassium chloride"}], "identifier": "ANDA209688", "issued": "2016-09-16", "keyword": ["medications", "health-care", "public-health", "prescription-drugs", "drug"], "landingPage": "https://www.fda.gov/drugs", "license": "https://open.fda.gov/license", "modified": "2025-03-17", "programCode": ["009:002"], "publisher": {"@type": "org:Organization", "name": "U.S. Food and Drug Administration"}, "theme": ["FDA"], "title": "Potassium chloride"}