{
  "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": "2026-10-08",
    "results": {
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  "results": [
    {
      "update_type": "Reverified",
      "initial_posting_date": "01/13/2022",
      "package_ndc": "76329-3302-1",
      "generic_name": "Dextrose Monohydrate 50% Injection",
      "contact_info": "800-423-4136",
      "availability": "Available",
      "openfda": {
        "application_number": [
          "ANDA203451"
        ],
        "brand_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "generic_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "manufacturer_name": [
          "International Medication Systems, Limited"
        ],
        "product_ndc": [
          "76329-3302"
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        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
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        "substance_name": [
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        "rxcui": [
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        "package_ndc": [
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        ],
        "unii": [
          "LX22YL083G"
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      },
      "update_date": "09/16/2026",
      "therapeutic_category": [
        "Endocrinology/Metabolism",
        "Gastroenterology",
        "Pediatric"
      ],
      "dosage_form": "Injection",
      "presentation": "Dextrose Monohydrate 50%, Injection, 25 g/50 mL (NDC 76329-3302-1)",
      "company_name": "Amphastar Pharmaceuticals, Inc.",
      "status": "Current"
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  ]
}