{
"NDC": {
"NDCCode": "50268-581-15",
"PackageDescription": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-581-15) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-581-11)",
"NDC11Code": "50268-0581-15",
"ProductNDC": "50268-581",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Mycophenolate Mofetil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Mycophenolate Mofetil",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20160825",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090456",
"LabelerName": "AvPAK",
"SubstanceName": "MYCOPHENOLATE MOFETIL",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antimetabolite Immunosuppressant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-04-12",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}