67253-821-55 : NDC 2026 Code

67253-821-55 : Hydrochlorothiazide ( Hydrochlorothiazide )

Additionally :

You can get information about “67253-821-55” NDC code in 67253-821-55 in HTML format

HTML | 67253-821-55 in TXT (Plain Text) format

TXT | 67253-821-55 in PDF (Portable Document Format)

PDF | 67253-821-55 in XML format

XML formats.

NDC Code : 67253-821-55 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "67253-821-55",
    "PackageDescription": "5000 TABLET in 1 BOTTLE (67253-821-55)",
    "NDC11Code": "67253-0821-55",
    "ProductNDC": "67253-821",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Hydrochlorothiazide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "19801105",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA087068",
    "LabelerName": "DAVA Pharmaceuticals, Inc.",
    "SubstanceName": "HYDROCHLOROTHIAZIDE",
    "StrengthNumber": "50",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2016-12-02",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}