{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Terminated",
      "city": "Horsham",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
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        "brand_name": [
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        "generic_name": [
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        "manufacturer_name": [
          "Teva Pharmaceuticals USA, Inc."
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        "product_ndc": [
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          "0093-4155",
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        "product_type": [
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        "route": [
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        "substance_name": [
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        "rxcui": [
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      "product_type": "Drugs",
      "event_id": "74540",
      "recalling_firm": "Teva North America",
      "address_1": "425 Privet Rd",
      "address_2": "",
      "postal_code": "19044-1220",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1470-2016",
      "product_description": "Amoxicillin for Oral Suspension USP, 400 mg/ 5 mL, 50 mL bottle, Rx only, Manufactured In Canada by: Teva Canada Limited, Toronto, Canada, NDC 0093-4161-76",
      "product_quantity": "53,328 bottles",
      "reason_for_recall": "Superpotent drug: Out of specification test result for assay during stability testing.",
      "recall_initiation_date": "20160624",
      "center_classification_date": "20160824",
      "termination_date": "20170207",
      "report_date": "20160831",
      "code_info": "Lot # 35434158A, Exp 6/17",
      "more_code_info": ""
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}