{
"NDC": {
"NDCCode": "50383-232-05",
"PackageDescription": "1 BOTTLE in 1 CARTON (50383-232-05) > 5 mL in 1 BOTTLE",
"NDC11Code": "50383-0232-05",
"ProductNDC": "50383-232",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Dorzolamide Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Dorzolamide Hydrochloride",
"DosageFormName": "SOLUTION/ DROPS",
"RouteName": "OPHTHALMIC",
"StartMarketingDate": "20081028",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077846",
"LabelerName": "Hi-Tech Pharmacal Co., Inc.",
"SubstanceName": "DORZOLAMIDE HYDROCHLORIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-06-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20081028",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}