68084-727-21 : NDC 2026 Code

68084-727-21 : Lisinopril And Hydrochlorothiazide ( Lisinopril And Hydrochlorothiazide )

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NDC Code : 68084-727-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68084-727-21",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-727-21)  &gt; 1 TABLET in 1 BLISTER PACK (68084-727-11)",
    "NDC11Code": "68084-0727-21",
    "ProductNDC": "68084-727",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lisinopril And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lisinopril And Hydrochlorothiazide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20140530",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077912",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "HYDROCHLOROTHIAZIDE; LISINOPRIL",
    "StrengthNumber": "12.5; 20",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-01-05",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}