{
"NDC": {
"NDCCode": "51079-196-03",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-196-03) > 1 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (51079-196-01)",
"NDC11Code": "51079-0196-03",
"ProductNDC": "51079-196",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Fenofibric Acid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Fenofibric Acid",
"DosageFormName": "CAPSULE, DELAYED RELEASE PELLETS",
"RouteName": "ORAL",
"StartMarketingDate": "20131121",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA200913",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "FENOFIBRIC ACID",
"StrengthNumber": "135",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2016-12-02",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}