{
"NDC": {
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"PackageDescription": "1 BLISTER PACK in 1 CARTON (51660-127-86) > 28 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "51660-0127-86",
"ProductNDC": "51660-127",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Norlyroc",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Norethindrone",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20140415",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA202260",
"LabelerName": "Ohm Laboratories Inc.",
"SubstanceName": "NORETHINDRONE",
"StrengthNumber": ".35",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Progesterone Congeners [CS],Progestin [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}