51079-570-05 : NDC 2026 Code

51079-570-05 : Methotrexate ( Methotrexate )

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NDC Code : 51079-570-05 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-570-05",
    "PackageDescription": "20 BLISTER PACK in 1 CARTON (51079-570-05)  &gt; 1 TABLET in 1 BLISTER PACK (51079-570-01) ",
    "NDC11Code": "51079-0570-05",
    "ProductNDC": "51079-570",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Methotrexate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Methotrexate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "19950712",
    "EndMarketingDate": "20300131",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA081235",
    "LabelerName": "Mylan Institutional Inc.",
    "SubstanceName": "METHOTREXATE SODIUM",
    "StrengthNumber": "2.5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2022-07-19",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "19950712",
    "EndMarketingDatePackage": "20300131",
    "SamplePackage": "N"
  }
}