{
  "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": "2026-09-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "68196-611",
      "generic_name": "acetaminophen",
      "labeler_name": "Sam's West Inc",
      "brand_name": "Members Mark Arthritis Pain",
      "active_ingredients": [
        {
          "name": "ACETAMINOPHEN",
          "strength": "650 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "68196-611-82",
          "description": "200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68196-611-82)",
          "marketing_start_date": "20251120",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Sam's West Inc"
        ],
        "rxcui": [
          "1148399"
        ],
        "spl_set_id": [
          "4cbe2880-fea9-4d7b-9e7f-a0c794864a84"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "362O9ITL9D"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
      "spl_id": "77d60018-88b8-4d09-8226-27c66ddce3da",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20251120",
      "product_id": "68196-611_77d60018-88b8-4d09-8226-27c66ddce3da",
      "application_number": "ANDA075077",
      "brand_name_base": "Members Mark Arthritis Pain"
    }
  ]
}