data.json

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            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "This list includes human and pet food subject to recall in the United States since January 2009 related to peanut products distributed by Peanut Corporation of America. ",
            "distribution": [
            {
                "downloadURL": "http://www.accessdata.fda.gov/scripts/peanutbutterrecall/PeanutButterProducts2009.xml",
                "mediaType": "application/xml",
                "accessURL": "http://www.accessdata.fda.gov/scripts/peanutbutterrecall/PeanutButterProducts2009.xml",
                "downloadURL": "http://www.accessdata.fda.gov/scripts/peanutbutterrecall/PeanutButterProducts2009.xml",
                "format": "XML"
            }
            ],
            "accrualPeriodicity": "irregular",
            "identifier": "5d4b366c-07ca-4358-a783-01aa2fe59684",
            "keyword": [
                "recalls"
            ],
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            "programCode": [
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            ],
            "publisher": {
                "name": "Office of Regulatory Affairs",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Peanut Product Recalls",
            "landingPage": "http://www.accessdata.fda.gov/scripts/peanutbutterrecall/PeanutButterProducts2009.xml"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "This list includes food subject to recall in the United States since March 2009 related to pistachios distributed by Setton Pistachio of Terra Bella, Inc. The FDA has completed its inspection of Salmonella contamination in pistachios and pistachio products involved in this recall. ",
            "distribution": [
            {
                "downloadURL": "http://www.accessdata.fda.gov/scripts/pistachiorecall/Pistachio2009.xml",
                "mediaType": "application/xml",
                "accessURL": "http://www.accessdata.fda.gov/scripts/pistachiorecall/Pistachio2009.xml",
                "downloadURL": "http://www.accessdata.fda.gov/scripts/pistachiorecall/Pistachio2009.xml",
                "format": "XML"
            }
            ],
            "accrualPeriodicity": "irregular",
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            "keyword": [
                "ora"
            ],
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            "publisher": {
                "name": "Office of Regulatory Affairs",
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                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Pistachio Product Recalls",
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        },
        {
            "accessLevel": "public",
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            ],
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                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "This list includes products subject to recall in the United States since February 2010 related to hydrolyzed vegetable protein (HVP) paste and powder distributed by Basic Food Flavors, Inc. HVP is a flavor enhancer used in a wide variety of processed food products such as soups, sauces, chilis, stews, hot dogs, gravies, seasoned snack foods, dips, and dressings. ",
            "distribution": [
            {
                "downloadURL": "http://www.accessdata.fda.gov/scripts/HVPCP/HydrolyzedVegetableProteinProductsList2010.xml",
                "mediaType": "application/xml",
                "accessURL": "http://www.accessdata.fda.gov/scripts/HVPCP/HydrolyzedVegetableProteinProductsList2010.xml",
                "downloadURL": "http://www.accessdata.fda.gov/scripts/HVPCP/HydrolyzedVegetableProteinProductsList2010.xml",
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            ],
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            ],
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            ],
            "publisher": {
                "name": "Office of Regulatory Affairs",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Hydrolyzed Vegetable Protein Containing Products Recalls",
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        },
        {
            "accessLevel": "public",
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                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "Epidemiologic investigations conducted by health officials in California, Colorado, and Minnesota revealed several restaurants or events where more than one person who fell ill with Salmonella Enteriditis had eaten. Information from these investigations suggested that shell eggs were the likely source of infections in many of these restaurants or events. And on August 13, 2010, Wright County Egg of Galt, Iowa, conducted a nationwide voluntary recalls of shell eggs that it had shipped since May 19, 2010. ",
            "distribution": [
            {
                "downloadURL": "http://www.accessdata.fda.gov/scripts/shelleggsrecall/ShellEggsRecallList2010.xml",
                "mediaType": "application/xml",
                "accessURL": "http://www.accessdata.fda.gov/scripts/shelleggsrecall/ShellEggsRecallList2010.xml",
                "downloadURL": "http://www.accessdata.fda.gov/scripts/shelleggsrecall/ShellEggsRecallList2010.xml",
                "format": "XML"
            }
            ],
            "accrualPeriodicity": "irregular",
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                "recalls"
            ],
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            ],
            "publisher": {
                "name": "Office of Regulatory Affairs",
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                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Shell Egg Recalls",
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        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "FDA Enterprise Data Inventory",
                "hasEmail": "mailto:FDA_Enterprise_Data_Inventory@fda.hhs.gov"
            },
            "description": "This system is a searchable repository of food code interpretations.  There are no exportable data sets.  All reports are in PDF format.  ",
            "distribution": [
            {
            }
            ],
            "identifier": "TBD by HHS",
            "keyword": [
                "food",
                "code",
                "interpretations"
            ],
            "modified": "2015-01-01",
            "programCode": [
                "009:001"
            ],
            "publisher": {
                "name": "      Center for Food Safety and Applied Nutrition",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Food Code Reference System"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "FDA Enterprise Data Inventory",
                "hasEmail": "mailto:FDA_Enterprise_Data_Inventory@fda.hhs.gov"
            },
            "description": "This system shares public data that can be downloaded.  ",
            "distribution": [
            {
            }
            ],
            "identifier": "8DFE05EA-9FA0-4DB8-B803-D3AA70564592",
            "keyword": [
                "Web Modules"
            ],
            "modified": "2014-09-12",
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                "009:001"
            ],
            "publisher": {
                "name": "      Center for Food Safety and Applied Nutrition",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "CFSAN Web Modules"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "FDA Enterprise Data Inventory",
                "hasEmail": "mailto:FDA_Enterprise_Data_Inventory@fda.hhs.gov"
            },
            "description": "This system supports the Information Center's Help Desk capabilities, and reports can be exported.  ",
            "distribution": [
            {
            }
            ],
            "identifier": "A6EEDE4E-01A2-4167-A196-87066F135C34",
            "keyword": [
                "Information Center; Foods Help Desk"
            ],
            "modified": "2014-12-01",
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            ],
            "publisher": {
                "name": "      Center for Food Safety and Applied Nutrition",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "CFSAN Knowledge Management System [is this salesforce?]"
        },
        {
            "accessLevel": "public",
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                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "This list includes products subject to recall since September 2010 related to infant formula distributed by Abbott. This list will be updated with publicly available information as received. The information is current as of the date indicated. If we learn that any information is not accurate, we will revise the list as soon as possible. When available, this database also includes photos of recalled products that have been voluntarily submitted by recalling firms to the FDA to assist the public in identifying those products that are subject to recall.",
            "distribution": [
            {
                "downloadURL": "http://www.accessdata.fda.gov/scripts/infantformula/InfantFormulaRecallList2010.xml",
                "mediaType": "application/xml",
                "accessURL": "http://www.accessdata.fda.gov/scripts/infantformula/InfantFormulaRecallList2010.xml",
                "downloadURL": "http://www.accessdata.fda.gov/scripts/infantformula/InfantFormulaRecallList2010.xml",
                "format": "XML"
            }
            ],
            "accrualPeriodicity": "irregular",
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            "keyword": [
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            ],
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            ],
            "publisher": {
                "name": "Office of Regulatory Affairs",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Abbott Infant Formula Recall",
            "landingPage": "http://www.accessdata.fda.gov/scripts/infantformula/InfantFormulaRecallList2010.xml"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "MedWatch alerts provide timely new safety information on human drugs, medical devices, vaccines and other biologics, dietary supplements, and cosmetics. The alerts contain actionable information that may impact both treatment and diagnostic choices for healthcare professional and patient.",
            "distribution": [
            {
                "downloadURL": "http://www.fda.gov/downloads/Safety/MedWatch/SafetyInformation/UCM189811.zip",
                "mediaType": "application/zip",
                "accessURL": "http://www.fda.gov/downloads/Safety/MedWatch/SafetyInformation/UCM189811.zip",
                "downloadURL": "http://www.fda.gov/downloads/Safety/MedWatch/SafetyInformation/UCM189811.zip",
                "format": "ZIP"
            }
            ],
            "accrualPeriodicity": "R/P1Y",
            "identifier": "2003711a-3d1c-4a0c-9928-09de5c42e2cf",
            "keyword": [
                "definitions"
            ],
            "modified": "R/P1Y",
            "programCode": [
                "009:008"
            ],
            "publisher": {
                "name": "Office of the Commissioner",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "MedWatch Safety Alerts for Human Medical Products",
            "landingPage": "http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/default.htm"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "FDA Enterprise Data Inventory",
                "hasEmail": "mailto:FDA_Enterprise_Data_Inventory@fda.hhs.gov"
            },
            "description": "Public access  allowing for public search of the FDA Adverse Events Database",
            "distribution": [
            {
                "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/ucm082193",
                "mediaType": "text/xml",
                "accessURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/ucm082193",
                "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/ucm082193",
                "format": "XML"
            }
            ],
            "identifier": "901A022F-A9B2-4B0A-9A33-0F3D353DF3FD",
            "keyword": [
                "FAERS"
            ],
            "modified": "2014-12-31",
            "programCode": [
                "009:002"
            ],
            "publisher": {
                "name": "OSE CDER",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Public Search for Adverse Events (FOIA)"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "Robert Reinwald",
                "hasEmail": "mailto:Robert.Reinwald@fda.hhs.gov"
            },
            "description": "The Approved Drug Products with Therapeutic Equivalence (Orange Book or OB) is a list of drugs approved under Section 505 of the Federal Food, Drug and Cosmetic Act and provides consumers timely updates on these products. In addition to these products (fo",
            "distribution": [
            {
            }
            ],
            "identifier": "5E4326F3-B3EC-40C7-B5B9-1115F3394E94",
            "keyword": [
                "Orange Book",
                "Approved Drug Products with Therapuetic Equivalence Evaluations"
            ],
            "modified": "2014-01-08",
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                "009:002"
            ],
            "publisher": {
                "name": "Food and Drug Administration",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Orange Book"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "Rajan, Velayudhan",
                "hasEmail": "mailto:Velayudhan.Rajan@fda.hhs.gov"
            },
            "description": "The Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). Unique device identification is a system being established by the",
            "distribution": [
            {
            }
            ],
            "identifier": "C37E5FDF-6717-4AB3-8585-1808C7BF3B3B",
            "keyword": [
                "cdrh",
                "udi",
                "gudid"
            ],
            "modified": "2014-02-04",
            "programCode": [
                "009:005"
            ],
            "publisher": {
                "name": "      Center for Devices and Radiological Health",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "GUDID Download"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "Danny Hsu",
                "hasEmail": "mailto:danny.hsu@fda.hhs.gov"
            },
            "description": "Harmful and Potentially Harmful Constituents",
            "distribution": [
            {
            }
            ],
            "identifier": "96E5B59F-286A-4127-A6E1-82EBA4981EFF",
            "keyword": [
                "HPHC",
                "Harmful",
                "Constituents"
            ],
            "modified": "2015-02-03",
            "programCode": [
                "009:007"
            ],
            "publisher": {
                "name": "    Food and Drug Administration",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Harmful and Potentially Harmful Constituents"
        },
        {
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            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "This application provides information for active, inactive, and pre-registered firms. Query options are by FEI, Applicant Name, Establishment Name, Other Names, Establishment Type, Establishment Status, City, State, Zip Code, Country and Reporting Official First Name or Last Name.",
            "distribution": [
            {
                "downloadURL": "https://www.accessdata.fda.gov/scripts/cber/CFAppsPub/",
                "mediaType": "text/html",
                "accessURL": "https://www.accessdata.fda.gov/scripts/cber/CFAppsPub/",
                "downloadURL": "https://www.accessdata.fda.gov/scripts/cber/CFAppsPub/",
                "format": "Interactive on-screen"
            }
            ],
            "identifier": "a0710f78-0585-45c8-9320-7d252b291390",
            "keyword": [
                "cber"
            ],
            "modified": "2010-06-04",
            "programCode": [
                "009:003"
            ],
            "publisher": {
                "name": "Center for Biologics Evaluation and Research",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Blood Establishment Registration Database",
            "landingPage": "https://www.accessdata.fda.gov/scripts/cber/CFAppsPub/"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "Provides information to the public on postmarket requirements and commitments. The phrase postmarket requirements and commitments refers to studies and clinical trials that sponsors conduct after approval to gather additional information about a product's safety, efficacy, or optimal use. Some of the studies and clinical trials may be required; others may be studies or clinical trials a sponsor has committed to conduct.",
            "distribution": [
            {
                "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Post-marketingPhaseIVCommitments/ucm070777.htm",
                "mediaType": "text/html",
                "accessURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Post-marketingPhaseIVCommitments/ucm070777.htm",
                "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Post-marketingPhaseIVCommitments/ucm070777.htm",
                "format": "Interactive on-screen"
            }
            ],
            "identifier": "bf085673-ae08-4807-8ca7-aeb36dde83ed",
            "keyword": [
                "cder"
            ],
            "modified": "2011-02-10",
            "programCode": [
                "009:002"
            ],
            "publisher": {
                "name": "Center for Drug Evaluation and Research",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Postmarket Requirements and Commitments",
            "landingPage": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm142931.htm"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "According to 21 CFR 210.3(b)(8), an inactive ingredient is any component of a drug product other than the active ingredient. Only inactive ingredients in the final dosage forms of drug products are in this database.",
            "distribution": [
            {
                "downloadURL": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm113978.htm",
                "mediaType": "application/zip",
                "accessURL": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm113978.htm",
                "downloadURL": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm113978.htm",
                "format": "Zip"
            }
            ],
            "identifier": "61f4a54b-daf5-4eb0-82fa-30dc89cd9699",
            "keyword": [
                "cder"
            ],
            "modified": "2013-01-02",
            "programCode": [
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            ],
            "publisher": {
                "name": "Center for Drug Evaluation and Research",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Inactive ingredient Search for Approved Drug Products",
            "describedBy": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm075230.htm",
            "landingPage": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm080123.htm"
        },
        {
            "accessLevel": "public",
            "bureauCode": [
                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products.",
            "distribution": [
            {
                "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm",
                "mediaType": "application/zip",
                "accessURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm",
                "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm",
                "format": "Zip"
            }
            ],
            "identifier": "c696c4f7-6de9-45db-988a-7195c2ade1d0",
            "keyword": [
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            ],
            "modified": "2013-08-16",
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            "publisher": {
                "name": "Center for Drug Evaluation and Research",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files",
            "landingPage": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm"
        },
        {
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                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "Information about FDA-approved brand name and generic prescription and over-the-counter human drugs and biological therapeutic products. Drugs@FDA includes most of the drug products approved since 1939. The majority of patient information, labels, approval letters, reviews, and other information are available for drug products approved since 1998.",
            "distribution": [
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                "downloadURL": "http://www.fda.gov/downloads/Drugs/InformationOnDrugs/UCM054599.zip",
                "mediaType": "application/zip",
                "accessURL": "http://www.fda.gov/downloads/Drugs/InformationOnDrugs/UCM054599.zip",
                "downloadURL": "http://www.fda.gov/downloads/Drugs/InformationOnDrugs/UCM054599.zip",
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            ],
            "accrualPeriodicity": "R/P1D",
            "identifier": "f22c9b6a-e68a-445a-ae44-1441b2f698ab",
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            "publisher": {
                "name": "Center for Drug Evaluation and Research",
                "subOrganizationOf": {
                    "name": "U.S. Food and Drug Administration"
                }
            },
            "title": "Drugs@FDA Database",
            "describedBy": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm079750.htm",
            "landingPage": "http://www.fda.gov/Drugs/InformationOnDrugs/ucm135821.htm"
        },
        {
            "accessLevel": "public",
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                "009:10"
            ],
            "contactPoint": {
                "fn": "openFDA",
                "hasEmail": "mailto:open@fda.hhs.gov"
            },
            "description": "The Drug Establishments Current Registration Site (DECRS) is a database of current information submitted by drug firms to register establishments (facilities) which manufacture, prepare, propagate, compound or process drugs that are commercially distributed in the U.S. or offered for import to the U.S.",
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            "description": "Contains data for FDA recalls from 2009 through the present.",
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            "title": "All FDA Recalls",
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            "description": "The National Health Related Items Code (NHRIC) is a system for identification and numbering of marketed device packages that is compatible with other numbering systems such as the National Drug Code (NDC) or Universal Product Code (UPC). Those manufacturers who desire to use the NHRIC number for unique product identification may apply to FDA for a labeler code. This database contains NHRIC data retrieved from records that date back 20 years.",
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            {
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                "downloadURL": "http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfNHRIC/nhric.cfm",
                "format": "Interactive on-screen"
            }
            ],
            "identifier": "72b6e176-fd0a-48eb-b373-38812dd98baa",
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            },
            "references": [
                "http://www.fda.gov/medicaldevices/deviceregulationandguidance/databases/ucm161456.htm"
            ],
            "title": "NHRIC (National Health Related Items Code)",
            "landingPage": "http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfNHRIC/nhric.cfm"
        },
        {
            "accessLevel": "public",
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            "contactPoint": {
                "fn": "openFDA",
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            "description": "This database allows you to search the CDRH's database information on medical devices which may have malfunctioned or caused a death or serious injury during the years 1992 through 1996.",
            "temporal": "1992-01-01/1996-07-31",
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            {
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                "accessURL": "http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmdr/search.CFM",
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            ],
            "title": "MDR (Medical Device Reporting)",
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        },
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            ],
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            "distribution": [
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            "description": "This database contains the commercially marketed in vitro test systems categorized by the FDA since January 31, 2000, and tests categorized by the Centers for Disease Control and Prevention (CDC) prior to that date.",
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            "description": "This database contains the most recent revision from the Government Printing Office (GPO) of the Code of Federal Regulations (CFR) Title 21 - Food and Drugs.",
            "distribution": [
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            "description": "This database contains historical information about CDRH Advisory Committees and Panel meetings through 2008, including summaries and transcripts. ",
            "temporal": "2001-01-01/2009-12-31",
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            "description": "An inventory of all FDA Datasets",
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            ],
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                "name": "Office of the Commissioner",
                "subOrganizationOf": {
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            "temporal": "2004-01-01/2012-12-31",
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            "description": "This list is intended to alert consumers about Web sites that are or were illegally marketing unapproved, uncleared, or unauthorized products in relation to the 2009 H1N1 Flu Virus (sometimes referred to as the 'swine flu' virus).",
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