70934-717-90 : NDC 2025 Code

70934-717-90 : Lisinopril And Hydrochlorothiazide ( Lisinopril And Hydrochlorothiazide )

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NDC Code : 70934-717-90 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70934-717-90",
    "PackageDescription": "90 TABLET in 1 BOTTLE, PLASTIC (70934-717-90) ",
    "NDC11Code": "70934-0717-90",
    "ProductNDC": "70934-717",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lisinopril And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lisinopril And Hydrochlorothiazide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200519",
    "EndMarketingDate": "20241130",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077912",
    "LabelerName": "Denton Pharma, Inc. dba Northwind Pharmaceuticals",
    "SubstanceName": "HYDROCHLOROTHIAZIDE; LISINOPRIL",
    "StrengthNumber": "12.5; 10",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-12-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20200519",
    "EndMarketingDatePackage": "20241130",
    "SamplePackage": "N"
  }
}