{
"NDC": {
"NDCCode": "72603-126-01",
"PackageDescription": "30 TABLET in 1 BOTTLE (72603-126-01) ",
"NDC11Code": "72603-0126-01",
"ProductNDC": "72603-126",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Vilazodone Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Vilazodone Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20230201",
"EndMarketingDate": "20241130",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA208209",
"LabelerName": "NorthStar RxLLC",
"SubstanceName": "VILAZODONE HYDROCHLORIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-12-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20230201",
"EndMarketingDatePackage": "20241130",
"SamplePackage": "N"
}
}