{
"NDC": {
"NDCCode": "50436-0255-1",
"PackageDescription": "50 POUCH in 1 BOX, UNIT-DOSE (50436-0255-1) > 1 TABLET, FILM COATED in 1 POUCH",
"NDC11Code": "50436-0255-01",
"ProductNDC": "50436-0255",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ropinirole",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ropinirole",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20100225",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090135",
"LabelerName": "Unit Dose Services",
"SubstanceName": "ROPINIROLE HYDROCHLORIDE",
"StrengthNumber": "1",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20180403",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}