{
"NDC": {
"NDCCode": "70518-2476-0",
"PackageDescription": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2476-0) ",
"NDC11Code": "70518-2476-00",
"ProductNDC": "70518-2476",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ropinirole Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ropinirole Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20191211",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078110",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "ROPINIROLE HYDROCHLORIDE",
"StrengthNumber": "1",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-09-14",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20191211",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}