{
  "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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    {
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      "generic_name": "Citric Acid and Sodium Citrate",
      "labeler_name": "CMP Pharma, Inc.",
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        {
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          "description": "500 mL in 1 BOTTLE (46287-014-01)",
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          "description": "10 BOTTLE, UNIT-DOSE in 1 CARTON (46287-014-15)  / 15 mL in 1 BOTTLE, UNIT-DOSE",
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      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
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      "dosage_form": "SOLUTION",
      "spl_id": "8691f6bc-18e9-4336-8e10-c702ecace00a",
      "product_type": "HUMAN PRESCRIPTION DRUG",
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      "product_id": "46287-014_8691f6bc-18e9-4336-8e10-c702ecace00a",
      "brand_name_base": "Oracit",
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        "Anti-coagulant [EPC]",
        "Calcium Chelating Activity [MoA]",
        "Calcium Chelating Activity [MoA]",
        "Calculi Dissolution Agent [EPC]",
        "Calculi Dissolution Agent [EPC]",
        "Decreased Coagulation Factor Activity [PE]",
        "Decreased Coagulation Factor Activity [PE]"
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}