{
"NDC": {
"NDCCode": "21695-914-40",
"PackageDescription": "1 VIAL in 1 CARTON (21695-914-40) > 40 mL in 1 VIAL",
"NDC11Code": "21695-0914-40",
"ProductNDC": "21695-914",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ciprofloxacin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ciprofloxacin",
"DosageFormName": "INJECTION, SOLUTION, CONCENTRATE",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20091208",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077245",
"LabelerName": "Rebel Distributors Corp",
"SubstanceName": "CIPROFLOXACIN",
"StrengthNumber": "400",
"StrengthUnit": "mg/40mL",
"Pharm_Classes": "Quinolone Antimicrobial [EPC],Quinolones [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}