50268-515-15 : NDC 2025 Code

50268-515-15 : Losartan Potassium And Hydrochlorothiazide ( Losartan Potassium And Hydrochlorothiazide )

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NDC Code : 50268-515-15 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50268-515-15",
    "PackageDescription": "50 BLISTER PACK in 1 BOX (50268-515-15)  &gt; 1 TABLET in 1 BLISTER PACK (50268-515-11) ",
    "NDC11Code": "50268-0515-15",
    "ProductNDC": "50268-515",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Losartan Potassium And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Losartan Potassium And Hydrochlorothiazide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20140414",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090528",
    "LabelerName": "AvPAK",
    "SubstanceName": "HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM",
    "StrengthNumber": "25; 100",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-08-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": "20140414",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}