{
"NDC": {
"NDCCode": "74458-157-01",
"PackageDescription": "200 mg in 1 BOTTLE (74458-157-01) ",
"NDC11Code": "74458-0157-01",
"ProductNDC": "74458-157",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Anti Dandruff",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ketoconazole",
"DosageFormName": "LIQUID",
"RouteName": "TOPICAL",
"StartMarketingDate": "20260704",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M032",
"LabelerName": "Guangzhou Yilong Cosmetics.,Ltd",
"SubstanceName": "KETOCONAZOLE",
"StrengthNumber": "1",
"StrengthUnit": "mg/100mg",
"Pharm_Classes": "Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2026-08-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260704",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}