46708-236-30 : NDC 2025 Code

46708-236-30 : Vardenafil Hydrochloride ( Vardenafil Hydrochloride )

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NDC Code : 46708-236-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "46708-236-30",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (46708-236-30) ",
    "NDC11Code": "46708-0236-30",
    "ProductNDC": "46708-236",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Vardenafil Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Vardenafil Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200805",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA214031",
    "LabelerName": "Alembic Pharmaceuticals Limited",
    "SubstanceName": "VARDENAFIL HYDROCHLORIDE",
    "StrengthNumber": "2.5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2023-01-26",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20200805",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}