{
"NDC": {
"NDCCode": "69367-354-10",
"PackageDescription": "1000 TABLET in 1 BOTTLE (69367-354-10) ",
"NDC11Code": "69367-0354-10",
"ProductNDC": "69367-354",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Metoprolol Tartrate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Metoprolol Tartrate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20231218",
"EndMarketingDate": "20260731",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074453",
"LabelerName": "Westminster Pharmaceuticals, LLC",
"SubstanceName": "METOPROLOL TARTRATE",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-12-06",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20231218",
"EndMarketingDatePackage": "20260731",
"SamplePackage": "N"
}
}