50268-742-15 : NDC 2025 Code

50268-742-15 : Ropinirole Hydrochloride ( Ropinirole Hydrochloride )

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NDC Code : 50268-742-15 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50268-742-15",
    "PackageDescription": "50 BLISTER PACK in 1 BOX (50268-742-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-742-11) ",
    "NDC11Code": "50268-0742-15",
    "ProductNDC": "50268-742",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ropinirole Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ropinirole Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220819",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078110",
    "LabelerName": "AvPAK",
    "SubstanceName": "ROPINIROLE HYDROCHLORIDE",
    "StrengthNumber": ".5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-01-11",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220819",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}