71626-999-08 : NDC 2026 Code

71626-999-08 : Probenecid ( Probenecid )

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NDC Code : 71626-999-08 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "71626-999-08",
    "PackageDescription": "8 TABLET, FILM COATED in 1 BOTTLE (71626-999-08) ",
    "NDC11Code": "71626-0999-08",
    "ProductNDC": "71626-999",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Probenecid",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Probenecid",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "19760729",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA080966",
    "LabelerName": "Medstone Pharma LLC",
    "SubstanceName": "PROBENECID",
    "StrengthNumber": "500",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2023-01-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20221231",
    "StartMarketingDatePackage": "20200904",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}