{
"NDC": {
"NDCCode": "59762-0800-2",
"PackageDescription": "60 TABLET, FILM COATED in 1 BOTTLE (59762-0800-2) ",
"NDC11Code": "59762-0800-02",
"ProductNDC": "59762-0800",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Tolterodine Tartrate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Tolterodine Tartrate",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20140121",
"EndMarketingDate": "20260731",
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA020771",
"LabelerName": "Mylan Pharmaceuticals Inc.",
"SubstanceName": "TOLTERODINE TARTRATE",
"StrengthNumber": "2",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-12-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20140121",
"EndMarketingDatePackage": "20260630",
"SamplePackage": "N"
}
}