{
"NDC": {
"NDCCode": "55154-5491-0",
"PackageDescription": "10 BLISTER PACK in 1 BAG (55154-5491-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "55154-5491-00",
"ProductNDC": "55154-5491",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Labetalol Hcl",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Labetalol Hcl",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20110506",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075113",
"LabelerName": "Cardinal Health",
"SubstanceName": "LABETALOL HYDROCHLORIDE",
"StrengthNumber": "200",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-11-16",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}