{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "11822-7892",
      "generic_name": "IBUPROFEN",
      "labeler_name": "RITE AID CORPORATION",
      "brand_name": "IBUPROFEN",
      "active_ingredients": [
        {
          "name": "IBUPROFEN",
          "strength": "200 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "11822-7892-0",
          "description": "24 TABLET, COATED in 1 BOTTLE (11822-7892-0)",
          "marketing_start_date": "20200601",
          "sample": false
        },
        {
          "package_ndc": "11822-7892-2",
          "description": "50 TABLET, COATED in 1 BOTTLE (11822-7892-2)",
          "marketing_start_date": "20200601",
          "sample": false
        },
        {
          "package_ndc": "11822-7892-5",
          "description": "100 TABLET, COATED in 1 BOTTLE (11822-7892-5)",
          "marketing_start_date": "20200601",
          "sample": false
        },
        {
          "package_ndc": "11822-7892-7",
          "description": "200 TABLET, COATED in 1 BOTTLE (11822-7892-7)",
          "marketing_start_date": "20200601",
          "sample": false
        },
        {
          "package_ndc": "11822-7892-9",
          "description": "500 TABLET, COATED in 1 BOTTLE (11822-7892-9)",
          "marketing_start_date": "20200601",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "RITE AID CORPORATION"
        ],
        "rxcui": [
          "310965"
        ],
        "spl_set_id": [
          "a7abac4c-7695-cfe8-e053-2a95a90ac1cd"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0011822789158",
          "0011822789141",
          "0011822789134",
          "0011822789127",
          "0011822789165"
        ],
        "nui": [
          "N0000000160",
          "M0001335",
          "N0000175722"
        ],
        "pharm_class_moa": [
          "Cyclooxygenase Inhibitors [MoA]"
        ],
        "pharm_class_cs": [
          "Anti-Inflammatory Agents, Non-Steroidal [CS]"
        ],
        "pharm_class_epc": [
          "Nonsteroidal Anti-inflammatory Drug [EPC]"
        ],
        "unii": [
          "WK2XYI10QM"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, COATED",
      "spl_id": "cf2caf6f-2192-2428-e053-2995a90aae6d",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20200601",
      "product_id": "11822-7892_cf2caf6f-2192-2428-e053-2995a90aae6d",
      "application_number": "ANDA091239",
      "brand_name_base": "IBUPROFEN",
      "pharm_class": [
        "Anti-Inflammatory Agents",
        "Non-Steroidal [CS]",
        "Cyclooxygenase Inhibitors [MoA]",
        "Nonsteroidal Anti-inflammatory Drug [EPC]"
      ]
    }
  ]
}