70518-1648-0 : NDC 2026 Code

70518-1648-0 : Olmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide ( Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide )

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NDC Code : 70518-1648-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-1648-0",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1648-0) ",
    "NDC11Code": "70518-1648-00",
    "ProductNDC": "70518-1648",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Olmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20181107",
    "EndMarketingDate": "20240630",
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA200175",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL",
    "StrengthNumber": "5; 25; 40",
    "StrengthUnit": "mg/1; mg/1; mg/1",
    "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2023-08-18",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20181107",
    "EndMarketingDatePackage": "20240630",
    "SamplePackage": "N"
  }
}