{
"NDC": {
"NDCCode": "70244-033-01",
"PackageDescription": "1 BOTTLE, DROPPER in 1 CARTON (70244-033-01) / 7.5 mL in 1 BOTTLE, DROPPER",
"NDC11Code": "70244-0033-01",
"ProductNDC": "70244-033",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ciprofloxacin And Dexamethasone",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ciprofloxacin And Dexamethasone",
"DosageFormName": "SUSPENSION/ DROPS",
"RouteName": "AURICULAR (OTIC)",
"StartMarketingDate": "20260416",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA215768",
"LabelerName": "Sentiss Pharmaceuticals LLC",
"SubstanceName": "CIPROFLOXACIN HYDROCHLORIDE; DEXAMETHASONE",
"StrengthNumber": "3; 1",
"StrengthUnit": "mg/mL; mg/mL",
"Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-04-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260416",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}