16571-885-09 : NDC 2025 Code

16571-885-09 : Allopurinol ( Allopurinol )

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NDC Code : 16571-885-09 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "16571-885-09",
    "PackageDescription": "90 TABLET in 1 BOTTLE (16571-885-09) ",
    "NDC11Code": "16571-0885-09",
    "ProductNDC": "16571-885",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Allopurinol",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Allopurinol",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20230921",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA016084",
    "LabelerName": "Rising Pharma Holdings, Inc.",
    "SubstanceName": "ALLOPURINOL",
    "StrengthNumber": "300",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2023-12-20",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20230921",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}