63739-357-33 : NDC 2026 Code

63739-357-33 : Valganciclovir Hydrochloride ( Valganciclovir Hydrochloride )

Additionally :

You can get information about “63739-357-33” NDC code in 63739-357-33 in HTML format

HTML | 63739-357-33 in TXT (Plain Text) format

TXT | 63739-357-33 in PDF (Portable Document Format)

PDF | 63739-357-33 in XML format

XML formats.

NDC Code : 63739-357-33 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-357-33",
    "PackageDescription": "3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-357-33)  / 10 TABLET in 1 BLISTER PACK",
    "NDC11Code": "63739-0357-33",
    "ProductNDC": "63739-357",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Valganciclovir Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Valganciclovir Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20160331",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA204750",
    "LabelerName": "Mckesson Corporation DBA SKY Packaginng",
    "SubstanceName": "VALGANCICLOVIR HYDROCHLORIDE",
    "StrengthNumber": "450",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], DNA Polymerase Inhibitors [MoA], Nucleoside Analog Antiviral [EPC], Nucleoside Analog [EXT]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-08-28",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20241231",
    "StartMarketingDatePackage": "20170531",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}