{
"NDC": {
"NDCCode": "52125-081-02",
"PackageDescription": "30 TABLET in 1 BLISTER PACK (52125-081-02)",
"NDC11Code": "52125-0081-02",
"ProductNDC": "52125-081",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nadolol",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Nadolol",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20130222",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074229",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "NADOLOL",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2016-12-27",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}