{
"NDC": {
"NDCCode": "82804-055-03",
"PackageDescription": "1 BOTTLE in 1 CARTON (82804-055-03) / 3 mL in 1 BOTTLE",
"NDC11Code": "82804-0055-03",
"ProductNDC": "82804-055",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Moxifloxacin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Moxifloxacin",
"DosageFormName": "SOLUTION/ DROPS",
"RouteName": "OPHTHALMIC",
"StartMarketingDate": "20171004",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA206242",
"LabelerName": "Proficient Rx LP",
"SubstanceName": "MOXIFLOXACIN HYDROCHLORIDE",
"StrengthNumber": "5",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2024-01-12",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20240109",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}