70518-0786-1 : NDC 2025 Code

70518-0786-1 : Losartan Potassium And Hydrochlorothiazide ( Losartan Potassium And Hydrochlorothiazide )

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NDC Code : 70518-0786-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-0786-1",
    "PackageDescription": "30 POUCH in 1 BOX (70518-0786-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-0786-2) ",
    "NDC11Code": "70518-0786-01",
    "ProductNDC": "70518-0786",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Losartan Potassium And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Losartan Potassium And Hydrochlorothiazide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20171012",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA091617",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM",
    "StrengthNumber": "25; 100",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-06-05",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20220310",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}