50742-331-30 : NDC 2026 Code

50742-331-30 : Pramipexole Dihydrochloride ( Pramipexole Dihydrochloride )

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NDC Code : 50742-331-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50742-331-30",
    "PackageDescription": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-331-30) ",
    "NDC11Code": "50742-0331-30",
    "ProductNDC": "50742-331",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Pramipexole Dihydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Pramipexole Dihydrochloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220310",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA213444",
    "LabelerName": "Ingenus Pharmaceuticals, LLC",
    "SubstanceName": "PRAMIPEXOLE DIHYDROCHLORIDE",
    "StrengthNumber": ".375",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-05-07",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220310",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}