61786-879-02 : NDC 2026 Code

61786-879-02 : Losartan Potassium And Hydrochlorothiazide ( Losartan Potassium And Hydrochlorothiazide )

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NDC Code : 61786-879-02 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "61786-879-02",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-879-02) ",
    "NDC11Code": "61786-0879-02",
    "ProductNDC": "61786-879",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Losartan Potassium And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Losartan Potassium And Hydrochlorothiazide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20160908",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA091629",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE",
    "StrengthNumber": "100; 25",
    "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": "2018-11-16",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20180501",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}