{
  "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": "2026-08-27",
    "results": {
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  "results": [
    {
      "discontinued_date": "03/26/2026",
      "update_type": "New",
      "initial_posting_date": "03/26/2026",
      "package_ndc": "39822-0350-2",
      "generic_name": "Lincomycin Hydrochloride Injection",
      "contact_info": "866-390-4411",
      "related_info": "A business decision was made to discontinue manufacture of the drug.",
      "openfda": {
        "application_number": [
          "ANDA201746"
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        "brand_name": [
          "LINCOMYCIN"
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        "generic_name": [
          "LINCOMYCIN HYDROCHLORIDE"
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        "manufacturer_name": [
          "XGen Pharmaceuticals DJB, Inc."
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          "39822-0353"
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          "INTRAVENOUS",
          "SUBCONJUNCTIVAL"
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        "substance_name": [
          "LINCOMYCIN HYDROCHLORIDE"
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      "update_date": "03/26/2026",
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      "dosage_form": "Injection",
      "presentation": "Lincomycin Hydrochloride, Injection, 600 mg/2 mL vial x 10 count (NDC 39822-0350-2)",
      "company_name": "XGen Pharmaceuticals DJB, Inc.",
      "status": "To Be Discontinued"
    }
  ]
}