{
  "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": "76420-803",
      "generic_name": "Benzonatate",
      "labeler_name": "Asclemed USA, Inc.",
      "brand_name": "Benzonatate",
      "active_ingredients": [
        {
          "name": "BENZONATATE",
          "strength": "100 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "76420-803-01",
          "description": "100 CAPSULE in 1 BOTTLE (76420-803-01)",
          "marketing_start_date": "20240429",
          "sample": false
        },
        {
          "package_ndc": "76420-803-05",
          "description": "500 CAPSULE in 1 BOTTLE (76420-803-05)",
          "marketing_start_date": "20240429",
          "sample": false
        },
        {
          "package_ndc": "76420-803-20",
          "description": "20 CAPSULE in 1 BOTTLE (76420-803-20)",
          "marketing_start_date": "20250418",
          "sample": false
        },
        {
          "package_ndc": "76420-803-30",
          "description": "30 CAPSULE in 1 BOTTLE (76420-803-30)",
          "marketing_start_date": "20240429",
          "sample": false
        },
        {
          "package_ndc": "76420-803-60",
          "description": "60 CAPSULE in 1 BOTTLE (76420-803-60)",
          "marketing_start_date": "20240429",
          "sample": false
        },
        {
          "package_ndc": "76420-803-90",
          "description": "90 CAPSULE in 1 BOTTLE (76420-803-90)",
          "marketing_start_date": "20240429",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Asclemed USA, Inc."
        ],
        "rxcui": [
          "197397",
          "283417"
        ],
        "spl_set_id": [
          "25ed5206-b322-486f-9e54-14125f6e74c5"
        ],
        "nui": [
          "N0000009010",
          "N0000175796"
        ],
        "pharm_class_pe": [
          "Decreased Tracheobronchial Stretch Receptor Activity [PE]"
        ],
        "pharm_class_epc": [
          "Non-narcotic Antitussive [EPC]"
        ],
        "unii": [
          "5P4DHS6ENR"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "CAPSULE",
      "spl_id": "3306a754-a59a-d003-e063-6294a90a65c9",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20181221",
      "product_id": "76420-803_3306a754-a59a-d003-e063-6294a90a65c9",
      "application_number": "ANDA206948",
      "brand_name_base": "Benzonatate",
      "pharm_class": [
        "Decreased Tracheobronchial Stretch Receptor Activity [PE]",
        "Non-narcotic Antitussive [EPC]"
      ]
    }
  ]
}