{
  "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": "57782-397",
      "generic_name": "Cromolyn Sodium",
      "labeler_name": "Bausch & Lomb Incorporated",
      "brand_name": "Cromolyn Sodium",
      "active_ingredients": [
        {
          "name": "CROMOLYN SODIUM",
          "strength": "5.2 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "57782-397-26",
          "description": "1 BOTTLE in 1 CARTON (57782-397-26)  / 200 SPRAY, METERED in 1 BOTTLE",
          "marketing_start_date": "20010703",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Bausch & Lomb Incorporated"
        ],
        "rxcui": [
          "1797851"
        ],
        "spl_set_id": [
          "379f4b59-6866-4b5c-9b1b-d8a35b741461"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "Q2WXR1I0PK"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "SPRAY, METERED",
      "spl_id": "d66445c2-3e1d-458a-9c62-d4fc2ef4ec8f",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "NASAL"
      ],
      "marketing_start_date": "20010703",
      "product_id": "57782-397_d66445c2-3e1d-458a-9c62-d4fc2ef4ec8f",
      "application_number": "ANDA075702",
      "brand_name_base": "Cromolyn Sodium",
      "pharm_class": [
        "Decreased Histamine Release [PE]",
        "Mast Cell Stabilizer [EPC]"
      ]
    }
  ]
}