{"@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": "Nebivolol Hydrochloride is a generic prescription medication available as oral tablets in strengths of 2.5 mg, 5 mg, 10 mg, and 20 mg. Manufactured by Novadoz Pharmaceuticals LLC, it belongs to the class of beta-adrenergic blockers, commonly used to treat high blood pressure. 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 Nebivolol \u2014 ANDA 217397 submitted by Mylan Institutional LLC\n    ", "downloadURL": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=217397", "mediaType": "text/html", "title": "Nebivolol"}], "identifier": "ANDA217397", "issued": "2016-09-16", "keyword": ["health-care", "drug-manufacturers", "drug", "pharmaceuticals", "drug-safety"], "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": "Nebivolol"}