{
  "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. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-22",
    "results": {
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  "results": [
    {
      "discontinued_date": "04/09/2026",
      "update_type": "New",
      "initial_posting_date": "04/09/2026",
      "package_ndc": "0069-4061-01",
      "generic_name": "Azithromycin Tablet",
      "contact_info": "800-533-4535",
      "related_info": "Discontinuation of the manufacture of the drug",
      "openfda": {
        "application_number": [
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        "brand_name": [
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        "generic_name": [
          "AZITHROMYCIN DIHYDRATE"
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        "manufacturer_name": [
          "Pfizer Laboratories Div Pfizer Inc"
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          "0069-3060",
          "0069-3070",
          "0069-3110",
          "0069-3120",
          "0069-3130",
          "0069-3140"
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        "route": [
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        "substance_name": [
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        "unii": [
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      "update_date": "04/09/2026",
      "therapeutic_category": [
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      "dosage_form": "Tablet",
      "presentation": "Zithromax, Tablet, 250 mg (NDC 0069-4061-01)",
      "company_name": "Pfizer Inc.",
      "status": "To Be Discontinued"
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  ]
}