0093-7239-56 : NDC 2026 Code

0093-7239-56 : Irbesartan And Hydrochlorothiazide ( Irbesartan And Hydrochlorothiazide )

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NDC Code : 0093-7239-56 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0093-7239-56",
    "PackageDescription": "30 TABLET in 1 BOTTLE (0093-7239-56)",
    "NDC11Code": "00093-7239-56",
    "ProductNDC": "0093-7239",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Irbesartan And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Irbesartan And Hydrochlorothiazide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20120330",
    "EndMarketingDate": "20140228",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077369",
    "LabelerName": "Teva Pharmaceuticals USA Inc",
    "SubstanceName": "HYDROCHLOROTHIAZIDE; IRBESARTAN",
    "StrengthNumber": "12.5; 300",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2014-03-05",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}