{
"NDC": {
"NDCCode": "51079-087-56",
"PackageDescription": "10 DOSE PACK in 1 CARTON (51079-087-56) > 30 BLISTER PACK in 1 DOSE PACK (51079-087-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-087-01) ",
"NDC11Code": "51079-0087-56",
"ProductNDC": "51079-087",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Mirtazapine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Mirtazapine",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20030801",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076122",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "MIRTAZAPINE",
"StrengthNumber": "30",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-02-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20080811",
"EndMarketingDatePackage": "20190131",
"SamplePackage": "N"
}
}