{
"NDC": {
"NDCCode": "67046-1489-3",
"PackageDescription": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1489-3) ",
"NDC11Code": "67046-1489-03",
"ProductNDC": "67046-1489",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ropinirole",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ropinirole",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20250129",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090429",
"LabelerName": "Coupler LLC",
"SubstanceName": "ROPINIROLE HYDROCHLORIDE",
"StrengthNumber": "2",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-01-31",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20250129",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}