51655-065-52 : NDC 2026 Code

51655-065-52 : Benazepril Hydrochloride ( Benazepril Hydrochloride )

Additionally :

You can get information about “51655-065-52” NDC code in 51655-065-52 in HTML format

HTML | 51655-065-52 in TXT (Plain Text) format

TXT | 51655-065-52 in PDF (Portable Document Format)

PDF | 51655-065-52 in XML format

XML formats.

NDC Code : 51655-065-52 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51655-065-52",
    "PackageDescription": "30 TABLET, COATED in 1 BOTTLE (51655-065-52) ",
    "NDC11Code": "51655-0065-52",
    "ProductNDC": "51655-065",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Benazepril Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Benazepril Hydrochloride",
    "DosageFormName": "TABLET, COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20160623",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076118",
    "LabelerName": "Northwind Health Company, LLC",
    "SubstanceName": "BENAZEPRIL HYDROCHLORIDE",
    "StrengthNumber": "10",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-02-19",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20160623",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}