{
"NDC": {
"NDCCode": "68084-205-01",
"PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-205-01) / 1 TABLET in 1 BLISTER PACK (68084-205-11) ",
"NDC11Code": "68084-0205-01",
"ProductNDC": "68084-205",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Minoxidil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Minoxidil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20070905",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA071839",
"LabelerName": "American Health Packaging",
"SubstanceName": "MINOXIDIL",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-12-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20070905",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}