{
"NDC": {
"NDCCode": "51079-821-56",
"PackageDescription": "10 DOSE PACK in 1 CARTON (51079-821-56) > 30 BLISTER PACK in 1 DOSE PACK (51079-821-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-821-01) ",
"NDC11Code": "51079-0821-56",
"ProductNDC": "51079-821",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Levetiracetam",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Levetiracetam",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20081104",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076919",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "LEVETIRACETAM",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Decreased Central Nervous System Disorganized Electrical Activity [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-12-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20081104",
"EndMarketingDatePackage": "20181130",
"SamplePackage": "N"
}
}