16571-706-10 : NDC 2025 Code

16571-706-10 : Topiramate ( Topiramate )

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NDC Code : 16571-706-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "16571-706-10",
    "PackageDescription": "1000 TABLET, FILM COATED in 1 BOTTLE (16571-706-10) ",
    "NDC11Code": "16571-0706-10",
    "ProductNDC": "16571-706",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Topiramate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Topiramate",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20090327",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078462",
    "LabelerName": "Rising Pharma Holdings, Inc.",
    "SubstanceName": "TOPIRAMATE",
    "StrengthNumber": "50",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-11-18",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220411",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}