55154-6837-0 : NDC 2026 Code

55154-6837-0 : Valacyclovir Hydrochloride ( Valacyclovir Hydrochloride )

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NDC Code : 55154-6837-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "55154-6837-0",
    "PackageDescription": "10 BLISTER PACK in 1 BAG (55154-6837-0)  &gt; 1 TABLET, FILM COATED in 1 BLISTER PACK",
    "NDC11Code": "55154-6837-00",
    "ProductNDC": "55154-6837",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Valacyclovir Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Valacyclovir Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20110523",
    "EndMarketingDate": "20201231",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090682",
    "LabelerName": "Cardinal Health",
    "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": "Deprecated",
    "LastUpdate": "2021-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20110523",
    "EndMarketingDatePackage": "20201231",
    "SamplePackage": "N"
  }
}