{
  "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": "2026-10-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "63323-873",
      "generic_name": "DEXTROSE MONOHYDRATE and SODIUM CHLORIDE",
      "labeler_name": "Fresenius Kabi USA, LLC",
      "brand_name": "Dextrose and Sodium Chloride",
      "active_ingredients": [
        {
          "name": "DEXTROSE MONOHYDRATE",
          "strength": "5 g/100mL"
        },
        {
          "name": "SODIUM CHLORIDE",
          "strength": ".225 g/100mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "63323-873-10",
          "description": "10 BAG in 1 CASE (63323-873-10)  / 1000 mL in 1 BAG (63323-873-01)",
          "marketing_start_date": "20201026",
          "sample": false
        },
        {
          "package_ndc": "63323-873-74",
          "description": "20 BAG in 1 CASE (63323-873-74)  / 500 mL in 1 BAG (63323-873-05)",
          "marketing_start_date": "20201026",
          "sample": false
        },
        {
          "package_ndc": "63323-873-75",
          "description": "30 BAG in 1 CASE (63323-873-75)  / 250 mL in 1 BAG (63323-873-15)",
          "marketing_start_date": "20201026",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Fresenius Kabi USA, LLC"
        ],
        "rxcui": [
          "1794902",
          "1794904",
          "1794905"
        ],
        "spl_set_id": [
          "df18a603-ca12-4b26-83b5-9dd07b6453ab"
        ],
        "is_original_packager": [
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        "unii": [
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          "451W47IQ8X"
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      "marketing_category": "ANDA",
      "dosage_form": "INJECTION, SOLUTION",
      "spl_id": "4ea28693-a341-402a-a8fa-b2a208ae6ab1",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
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      "marketing_start_date": "20201026",
      "product_id": "63323-873_4ea28693-a341-402a-a8fa-b2a208ae6ab1",
      "application_number": "ANDA211221",
      "brand_name_base": "Dextrose and Sodium Chloride",
      "pharm_class": [
        "Increased Large Intestinal Motility [PE]",
        "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]",
        "Osmotic Activity [MoA]",
        "Osmotic Laxative [EPC]"
      ]
    }
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}