76420-459-07 : NDC 2026 Code

76420-459-07 : Valacyclovir Hydrochloride ( Valacyclovir Hydrochloride )

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NDC Code : 76420-459-07 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "76420-459-07",
    "PackageDescription": "7 TABLET, FILM COATED in 1 BOTTLE (76420-459-07) ",
    "NDC11Code": "76420-0459-07",
    "ProductNDC": "76420-459",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Valacyclovir Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Valacyclovir Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20100524",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090682",
    "LabelerName": "ASCLEMED USA INC.",
    "SubstanceName": "VALACYCLOVIR HYDROCHLORIDE",
    "StrengthNumber": "500",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-10-23",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250817",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}