{
  "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": "2026-09-25",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "51655-539",
      "generic_name": "cyclobenzaprine hydrochloride",
      "labeler_name": "Northwind Health Company, LLC",
      "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE",
      "active_ingredients": [
        {
          "name": "CYCLOBENZAPRINE HYDROCHLORIDE",
          "strength": "10 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "51655-539-20",
          "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-20)",
          "marketing_start_date": "20210114",
          "sample": false
        },
        {
          "package_ndc": "51655-539-52",
          "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-52)",
          "marketing_start_date": "20210526",
          "sample": false
        },
        {
          "package_ndc": "51655-539-53",
          "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-53)",
          "marketing_start_date": "20220415",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Northwind Health Company, LLC"
        ],
        "rxcui": [
          "828348"
        ],
        "spl_set_id": [
          "dae3be94-a40c-5be1-e053-2a95a90a1484"
        ],
        "unii": [
          "0VE05JYS2P"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, FILM COATED",
      "spl_id": "494dea9c-f9af-2eec-e063-6294a90ab96f",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20210114",
      "product_id": "51655-539_494dea9c-f9af-2eec-e063-6294a90ab96f",
      "application_number": "ANDA208170",
      "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE",
      "pharm_class": [
        "Centrally-mediated Muscle Relaxation [PE]",
        "Muscle Relaxant [EPC]"
      ]
    }
  ]
}