63629-5233-1 : NDC 2026 Code

63629-5233-1 : Candesartan Cilexetil And Hydrochlorothiazide ( Candesartan Cilexetil And Hydrochlorothiazide )

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NDC Code : 63629-5233-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63629-5233-1",
    "PackageDescription": "30 TABLET in 1 BOTTLE (63629-5233-1)",
    "NDC11Code": "63629-5233-01",
    "ProductNDC": "63629-5233",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Candesartan Cilexetil And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Candesartan Cilexetil And Hydrochlorothiazide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20121204",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA202884",
    "LabelerName": "Bryant Ranch Prepack",
    "SubstanceName": "CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE",
    "StrengthNumber": "16; 12.5",
    "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": "2017-06-08",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}