68462-576-01 : NDC 2026 Code

68462-576-01 : Benazepril Hydrochloride And Hydrochlorothiazide ( Benazepril Hydrochloride And Hydrochlorothiazide )

Additionally :

You can get information about “68462-576-01” NDC code in 68462-576-01 in HTML format

HTML | 68462-576-01 in TXT (Plain Text) format

TXT | 68462-576-01 in PDF (Portable Document Format)

PDF | 68462-576-01 in XML format

XML formats.

NDC Code : 68462-576-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68462-576-01",
    "PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE (68462-576-01) ",
    "NDC11Code": "68462-0576-01",
    "ProductNDC": "68462-576",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Benazepril Hydrochloride And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Benazepril Hydrochloride And Hydrochlorothiazide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20150317",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076631",
    "LabelerName": "Glenmark Pharmaceuticals Inc., USA",
    "SubstanceName": "BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE",
    "StrengthNumber": "5; 6.25",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2023-12-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20231201",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}