{
  "name": "FDA-Approved Testosterone Brands, 2026",
  "dateModified": "2026-09-02",
  "methodologyNote": "Unique current proprietary names are counted once. Separate FDA applications/formulations are counted as separate records. Product status follows FDA records on the verification date.",
  "records": [
    {
      "Brand": "Depo-Testosterone",
      "FDA application": "NDA 018386",
      "Verified correction": "Original approval: July 25, 1979",
      "FDA record": "018386",
      "Audit note": "FDA application date corrected from an imprecise “before 1982” value.",
      "Primary FDA source": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=018386"
    },
    {
      "Brand": "Testopel",
      "FDA application": "NDA 009165",
      "Verified correction": "Current application approval: July 13, 1972",
      "FDA record": "009165",
      "Audit note": "Uses the current NDA record date; 1942 belongs only in product-history context.",
      "Primary FDA source": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=009165"
    },
    {
      "Brand": "Kyzatrex",
      "FDA application": "NDA 213953",
      "Verified correction": "Current strengths: 150 mg and 200 mg; 100 mg is discontinued",
      "FDA record": "213953",
      "Audit note": "The 100 mg strength is discontinued; current strengths are 150 mg and 200 mg.",
      "Primary FDA source": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=213953"
    },
    {
      "Brand": "Testim",
      "FDA application": "NDA 021454",
      "Verified correction": "Current FDA product form: packet",
      "FDA record": "021454",
      "Audit note": "FDA lists the branded product as a packet, not a tube.",
      "Primary FDA source": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=021454"
    },
    {
      "Brand": "Vogelxo",
      "FDA application": "NDA 204399",
      "Verified correction": "Current FDA products: packet and metered-dose pump",
      "FDA record": "204399",
      "Audit note": "Current FDA record shows a packet and metered-dose pump; no current tube listing.",
      "Primary FDA source": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204399"
    }
  ]
}