{
"NDC": {
"NDCCode": "42291-618-90",
"PackageDescription": "90 TABLET in 1 BOTTLE (42291-618-90) ",
"NDC11Code": "42291-0618-90",
"ProductNDC": "42291-618",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Minoxidil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Minoxidil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20130801",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA072708",
"LabelerName": "AvKARE, Inc.",
"SubstanceName": "MINOXIDIL",
"StrengthNumber": "2.5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-04-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20130801",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}