{
  "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": "2026-10-09",
    "results": {
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    {
      "product_ndc": "76297-006",
      "generic_name": "Trisodium Citrate Dihydrate",
      "labeler_name": "LABORATORIOS GRIFOLS SA",
      "brand_name": "Anticoagulant Sodium Citrate",
      "active_ingredients": [
        {
          "name": "TRISODIUM CITRATE DIHYDRATE",
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      "finished": true,
      "packaging": [
        {
          "package_ndc": "76297-006-03",
          "description": "30 BAG in 1 CARTON (76297-006-03)  / 250 mL in 1 BAG (76297-006-02)",
          "marketing_start_date": "20191025",
          "sample": false
        },
        {
          "package_ndc": "76297-006-04",
          "description": "39 BAG in 1 CARTON (76297-006-04)  / 250 mL in 1 BAG (76297-006-02)",
          "marketing_start_date": "20191025",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
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      "marketing_category": "ANDA",
      "dosage_form": "SOLUTION",
      "spl_id": "fa83d193-9cfc-40c0-b924-b1685c50d08a",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
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      "application_number": "BA125697",
      "brand_name_base": "Anticoagulant Sodium Citrate",
      "pharm_class": [
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        "Anti-coagulant [EPC]",
        "Calcium Chelating Activity [MoA]",
        "Calculi Dissolution Agent [EPC]",
        "Decreased Coagulation Factor Activity [PE]"
      ]
    }
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}