{
"NDC": {
"NDCCode": "39822-0190-7",
"PackageDescription": "1 VIAL, GLASS in 1 CARTON (39822-0190-7) > 5 mL in 1 VIAL, GLASS",
"NDC11Code": "39822-0190-07",
"ProductNDC": "39822-0190",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Acetazolamide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Acetazolamide",
"DosageFormName": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20131210",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040784",
"LabelerName": "X-GEN Pharmaceuticals, Inc.",
"SubstanceName": "ACETAZOLAMIDE SODIUM",
"StrengthNumber": "500",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-01-22",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20211231",
"StartMarketingDatePackage": "20140801",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}