{
  "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": "2026-10-02",
    "results": {
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      "generic_name": "Diatrizoate Meglumine and Diatrizoate Sodium",
      "labeler_name": "Camber Pharmaceuticals, Inc.",
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      "active_ingredients": [
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          "description": "24 BOTTLE in 1 BOX (31722-019-31)  / 30 mL in 1 BOTTLE (31722-019-30)",
          "marketing_start_date": "20231117",
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        {
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          "description": "12 BOTTLE in 1 BOX (31722-019-32)  / 120 mL in 1 BOTTLE (31722-019-12)",
          "marketing_start_date": "20231117",
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      ],
      "listing_expiration_date": "20261231",
      "openfda": {
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      "spl_id": "2e7917f2-e573-cccb-e063-6294a90a203c",
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      "marketing_start_date": "20231117",
      "product_id": "31722-019_2e7917f2-e573-cccb-e063-6294a90a203c",
      "application_number": "ANDA215049",
      "brand_name_base": "Diatrizoate Meglumine and Diatrizoate Sodium",
      "pharm_class": [
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        "Radiographic Contrast Agent [EPC]",
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        "X-Ray Contrast Activity [MoA]"
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}