{
"NDC": {
"NDCCode": "50436-0656-1",
"PackageDescription": "1 BOTTLE in 1 CARTON (50436-0656-1) > 5 mL in 1 BOTTLE",
"NDC11Code": "50436-0656-01",
"ProductNDC": "50436-0656",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ciprofloxacin Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ciprofloxacin Hydrochloride",
"DosageFormName": "SOLUTION/ DROPS",
"RouteName": "OPHTHALMIC",
"StartMarketingDate": "20040507",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA019992",
"LabelerName": "Unit Dose Services",
"SubstanceName": "CIPROFLOXACIN HYDROCHLORIDE",
"StrengthNumber": "3",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Quinolone Antimicrobial [EPC],Quinolones [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20180810",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}