{
"NDC": {
"NDCCode": "55545-1008-2",
"PackageDescription": "1 BOTTLE in 1 CARTON (55545-1008-2) > 10 mL in 1 BOTTLE",
"NDC11Code": "55545-1008-02",
"ProductNDC": "55545-1008",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Dorzolamide Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Dorzolamide Hydrochloride",
"DosageFormName": "SOLUTION",
"RouteName": "OPHTHALMIC",
"StartMarketingDate": "20191116",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA205294",
"LabelerName": "FDC Limited",
"SubstanceName": "DORZOLAMIDE HYDROCHLORIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-01-24",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20191116",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}