58602-706-41 : NDC 2026 Code

58602-706-41 : Famotidine ( Famotidine )

Additionally :

You can get information about “58602-706-41” NDC code in 58602-706-41 in HTML format

HTML | 58602-706-41 in TXT (Plain Text) format

TXT | 58602-706-41 in PDF (Portable Document Format)

PDF | 58602-706-41 in XML format

XML formats.

NDC Code : 58602-706-41 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "58602-706-41",
    "PackageDescription": "1000 TABLET, FILM COATED in 1 BOTTLE (58602-706-41) ",
    "NDC11Code": "58602-0706-41",
    "ProductNDC": "58602-706",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Famotidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Famotidine",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20160426",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA206531",
    "LabelerName": "Aurohealth LLC",
    "SubstanceName": "FAMOTIDINE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-04-24",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20200904",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}