81469-353-05 : NDC 2026 Code

81469-353-05 : Cetirizine Hydrochloride ( Cetirizine Hydrochloride )

Additionally :

You can get information about “81469-353-05” NDC code in 81469-353-05 in HTML format

HTML | 81469-353-05 in TXT (Plain Text) format

TXT | 81469-353-05 in PDF (Portable Document Format)

PDF | 81469-353-05 in XML format

XML formats.

NDC Code : 81469-353-05 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "81469-353-05",
    "PackageDescription": "500 TABLET in 1 BOTTLE (81469-353-05) ",
    "NDC11Code": "81469-0353-05",
    "ProductNDC": "81469-353",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Cetirizine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Cetirizine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20260529",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076047",
    "LabelerName": "First Nation Group, LLC",
    "SubstanceName": "CETIRIZINE HYDROCHLORIDE",
    "StrengthNumber": "10",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-06-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260601",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}