{
"NDC": {
"NDCCode": "49349-654-02",
"PackageDescription": "30 TABLET in 1 BLISTER PACK (49349-654-02)",
"NDC11Code": "49349-0654-02",
"ProductNDC": "49349-654",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Minoxidil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Minoxidil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20110518",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA071826",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "MINOXIDIL",
"StrengthNumber": "2.5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-02-17",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}