{
"NDC": {
"NDCCode": "0904-7226-04",
"PackageDescription": "30 BLISTER PACK in 1 CARTON (0904-7226-04) / 1 TABLET in 1 BLISTER PACK",
"NDC11Code": "00904-7226-04",
"ProductNDC": "0904-7226",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nebivolol",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Nebivolol",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20180302",
"EndMarketingDate": "20251130",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA203966",
"LabelerName": "Major Pharmaceuticals",
"SubstanceName": "NEBIVOLOL HYDROCHLORIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-12-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20180302",
"EndMarketingDatePackage": "20251130",
"SamplePackage": "N"
}
}