{
"NDC": {
"NDCCode": "70518-1398-1",
"PackageDescription": "20 TABLET in 1 BOTTLE, PLASTIC (70518-1398-1) ",
"NDC11Code": "70518-1398-01",
"ProductNDC": "70518-1398",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Methotrexate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Methotrexate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20180904",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA207812",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "METHOTREXATE",
"StrengthNumber": "2.5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-04-20",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20180930",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}