{
  "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": "50844-714",
      "generic_name": "Naproxen Sodium",
      "labeler_name": "L.N.K. International, Inc.",
      "brand_name": "Naproxen Back and Muscle Pain",
      "active_ingredients": [
        {
          "name": "NAPROXEN SODIUM",
          "strength": "220 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "50844-714-14",
          "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)",
          "marketing_start_date": "20190201",
          "sample": false
        },
        {
          "package_ndc": "50844-714-16",
          "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16)",
          "marketing_start_date": "20190201",
          "sample": false
        },
        {
          "package_ndc": "50844-714-19",
          "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19)  / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC",
          "marketing_start_date": "20190201",
          "sample": false
        },
        {
          "package_ndc": "50844-714-56",
          "description": "25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56)",
          "marketing_start_date": "20190201",
          "sample": false
        },
        {
          "package_ndc": "50844-714-98",
          "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98)",
          "marketing_start_date": "20190201",
          "sample": false
        },
        {
          "package_ndc": "50844-714-99",
          "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)",
          "marketing_start_date": "20190201",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "L.N.K. International, Inc."
        ],
        "rxcui": [
          "849574"
        ],
        "spl_set_id": [
          "68944663-0dc0-4d3a-a36b-019061bdbfa0"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0350844714169"
        ],
        "unii": [
          "9TN87S3A3C"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, FILM COATED",
      "spl_id": "bc397444-6e0e-4b4e-8f03-d6372588d8ab",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20190201",
      "product_id": "50844-714_bc397444-6e0e-4b4e-8f03-d6372588d8ab",
      "application_number": "ANDA204872",
      "brand_name_base": "Naproxen Back and Muscle Pain",
      "pharm_class": [
        "Anti-Inflammatory Agents",
        "Non-Steroidal [CS]",
        "Cyclooxygenase Inhibitors [MoA]",
        "Nonsteroidal Anti-inflammatory Drug [EPC]"
      ]
    }
  ]
}