55289-086-30 : NDC 2026 Code

55289-086-30 : Benazepril Hydrochloride ( Lotensin )

Additionally :

You can get information about “55289-086-30” NDC code in 55289-086-30 in HTML format

HTML | 55289-086-30 in TXT (Plain Text) format

TXT | 55289-086-30 in PDF (Portable Document Format)

PDF | 55289-086-30 in XML format

XML formats.

NDC Code : 55289-086-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "55289-086-30",
    "PackageDescription": "30 TABLET in 1 BOTTLE, PLASTIC (55289-086-30)",
    "NDC11Code": "55289-0086-30",
    "ProductNDC": "55289-086",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lotensin",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Benazepril Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "19910625",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA019851",
    "LabelerName": "PD-Rx Pharmaceuticals, Inc.",
    "SubstanceName": "BENAZEPRIL HYDROCHLORIDE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2016-12-22",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}