{"@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": "Furosemide is a prescription loop diuretic used to treat conditions like edema (fluid retention) and high blood pressure by increasing urine production. This injectable solution (10 mg/mL) is administered intravenously and comes in 4 mL single-dose vials, packaged in boxes of 25. Manufactured by Baxter Healthcare Corporation and Civica, Inc., under application ANDA202747. 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 Furosemide \u2014 ANDA 214766 submitted by Mylan Institutional LLC\n    ", "downloadURL": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=214766", "mediaType": "text/html", "title": "Furosemide"}], "identifier": "ANDA214766", "issued": "2016-09-16", "keyword": ["medications", "health-care", "fda", "drug-safety", "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": "Furosemide"}