{
"NDC": {
"NDCCode": "52125-855-01",
"PackageDescription": "1 TUBE, WITH APPLICATOR in 1 CARTON (52125-855-01) > 70 g in 1 TUBE, WITH APPLICATOR",
"NDC11Code": "52125-0855-01",
"ProductNDC": "52125-855",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Metronidazole",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Metronidazole",
"DosageFormName": "GEL",
"RouteName": "VAGINAL",
"StartMarketingDate": "20140228",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077264",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "METRONIDAZOLE",
"StrengthNumber": "7.5",
"StrengthUnit": "mg/g",
"Pharm_Classes": "Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-02-17",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}