{
"NDC": {
"NDCCode": "51672-1308-3",
"PackageDescription": "1 BOTTLE in 1 CARTON (51672-1308-3) / 30 mL in 1 BOTTLE",
"NDC11Code": "51672-1308-03",
"ProductNDC": "51672-1308",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Clotrimazole And Betamethasone Dipropionate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Clotrimazole And Betamethasone Dipropionate",
"DosageFormName": "LOTION",
"RouteName": "TOPICAL",
"StartMarketingDate": "20040728",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076493",
"LabelerName": "Sun Pharmaceutical Industries, Inc.",
"SubstanceName": "BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE",
"StrengthNumber": ".5; 10",
"StrengthUnit": "mg/mL; mg/mL",
"Pharm_Classes": "Azole Antifungal [EPC], Azoles [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-07-08",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20040728",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}