{
  "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": {
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      "limit": 1,
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      "generic_name": "Diclofenac Sodium/Misoprostol",
      "labeler_name": "Micro Labs Limited",
      "brand_name": "Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL",
      "brand_name_suffix": "DICLOFENAC-SODIUM-MISOPROSTOL",
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        {
          "name": "DICLOFENAC SODIUM",
          "strength": "50 mg/1"
        },
        {
          "name": "MISOPROSTOL",
          "strength": "200 ug/1"
        }
      ],
      "finished": true,
      "packaging": [
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          "description": "60 BLISTER PACK in 1 CARTON (42571-133-29)  / 10 TABLET in 1 BLISTER PACK",
          "marketing_start_date": "20210901",
          "sample": false
        },
        {
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          "description": "30 TABLET in 1 BOTTLE (42571-133-30)",
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        },
        {
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        },
        {
          "package_ndc": "42571-133-90",
          "description": "90 TABLET in 1 BOTTLE (42571-133-90)",
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          "sample": false
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      ],
      "listing_expiration_date": "20261231",
      "openfda": {
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          "0342571134600"
        ],
        "nui": [
          "N0000175785",
          "M0017811"
        ],
        "pharm_class_epc": [
          "Prostaglandin E1 Analog [EPC]"
        ],
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      "application_number": "ANDA204355",
      "brand_name_base": "Diclofenac Sodium/Misoprostol",
      "pharm_class": [
        "Anti-Inflammatory Agents",
        "Non-Steroidal [CS]",
        "Cyclooxygenase Inhibitors [MoA]",
        "Decreased Prostaglandin Production [PE]",
        "Nonsteroidal Anti-inflammatory Drug [EPC]",
        "Prostaglandin E1 Analog [EPC]",
        "Prostaglandins E",
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}