{
"NDC": {
"NDCCode": "59212-087-30",
"PackageDescription": "30 TABLET in 1 BOTTLE (59212-087-30) ",
"NDC11Code": "59212-0087-30",
"ProductNDC": "59212-087",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Dutoprol",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Metoprolol Succinate And Hydrochlorothiazide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20140701",
"EndMarketingDate": "20220331",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA021956",
"LabelerName": "Concordia Pharmaceuticals Inc.",
"SubstanceName": "HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE",
"StrengthNumber": "12.5; 25",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-04-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20140701",
"EndMarketingDatePackage": "20220331",
"SamplePackage": "N"
}
}