{
  "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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  "results": [
    {
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      "generic_name": "ALBUMIN (HUMAN)",
      "labeler_name": "GRIFOLS USA, LLC",
      "brand_name": "HUMAN ALBUMIN GRIFOLS",
      "active_ingredients": [
        {
          "name": "ALBUMIN HUMAN",
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      "packaging": [
        {
          "package_ndc": "61953-0001-2",
          "description": "1 VIAL in 1 CARTON (61953-0001-2)  / 100 mL in 1 VIAL (61953-0001-4)",
          "marketing_start_date": "19950217",
          "sample": false
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      "openfda": {},
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      "product_type": "PLASMA DERIVATIVE",
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      "product_id": "61953-0001_23b658d2-a395-40f9-b894-1a708b2d12ad",
      "application_number": "BLA103352",
      "brand_name_base": "HUMAN ALBUMIN GRIFOLS",
      "pharm_class": [
        "Human Serum Albumin [EPC]",
        "Increased Intravascular Volume [PE]",
        "Increased Oncotic Pressure [PE]",
        "Osmotic Activity [MoA]",
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}