71335-1772-1 : NDC 2025 Code

71335-1772-1 : Methotrexate ( Methotrexate )

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NDC Code : 71335-1772-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "71335-1772-1",
    "PackageDescription": "30 TABLET in 1 BOTTLE (71335-1772-1) ",
    "NDC11Code": "71335-1772-01",
    "ProductNDC": "71335-1772",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Methotrexate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Methotrexate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200824",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA213343",
    "LabelerName": "Bryant Ranch Prepack",
    "SubstanceName": "METHOTREXATE SODIUM",
    "StrengthNumber": "2.5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-05-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20211229",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}