{
  "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": "2026-09-18",
    "results": {
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  "results": [
    {
      "update_type": "Reverified",
      "initial_posting_date": "11/03/2023",
      "package_ndc": "42571-132-52",
      "generic_name": "Cromolyn Sodium Concentrate",
      "contact_info": "(908) 484-7410",
      "availability": "Available",
      "openfda": {
        "application_number": [
          "ANDA202745"
        ],
        "brand_name": [
          "CROMOLYN SODIUM"
        ],
        "generic_name": [
          "CROMOLYN SODIUM"
        ],
        "manufacturer_name": [
          "Micro Labs Limited"
        ],
        "product_ndc": [
          "42571-132"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
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        "substance_name": [
          "CROMOLYN SODIUM"
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        "rxcui": [
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        "spl_id": [
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          "42571-132-52"
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        "unii": [
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      },
      "update_date": "09/16/2026",
      "therapeutic_category": [
        "Pulmonary/Allergy"
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      "dosage_form": "Concentrate",
      "presentation": "Cromolyn Sodium, Concentrate, 100 mg/5 mL (NDC 42571-132-52)",
      "company_name": "Micro Labs LTD",
      "status": "Current"
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}