{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "70518-0860",
      "generic_name": "Pantoprazole Sodium",
      "labeler_name": "REMEDYREPACK INC.",
      "brand_name": "Pantoprazole Sodium",
      "active_ingredients": [
        {
          "name": "PANTOPRAZOLE SODIUM",
          "strength": "40 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "70518-0860-0",
          "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0860-0)",
          "marketing_start_date": "20171120",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "REMEDYREPACK INC."
        ],
        "rxcui": [
          "314200"
        ],
        "spl_set_id": [
          "f313159c-115a-4cf6-b32e-9ddc833fd51c"
        ],
        "unii": [
          "6871619Q5X"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, DELAYED RELEASE",
      "spl_id": "558edbda-5dba-a843-e063-6294a90a09a6",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20171120",
      "product_id": "70518-0860_558edbda-5dba-a843-e063-6294a90a09a6",
      "application_number": "ANDA202038",
      "brand_name_base": "Pantoprazole Sodium",
      "pharm_class": [
        "Proton Pump Inhibitor [EPC]",
        "Proton Pump Inhibitors [MoA]"
      ]
    }
  ]
}