75834-230-10 : NDC 2026 Code

75834-230-10 : Remifentanil Hydrochloride ( Remifentanil Hydrochloride )

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NDC Code : 75834-230-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "75834-230-10",
    "PackageDescription": "10 VIAL, GLASS in 1 CARTON (75834-230-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS (75834-230-01) ",
    "NDC11Code": "75834-0230-10",
    "ProductNDC": "75834-230",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Remifentanil Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Remifentanil Hydrochloride",
    "DosageFormName": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
    "RouteName": "INTRAVENOUS",
    "StartMarketingDate": "20240904",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA215635",
    "LabelerName": "Nivagen Pharmaceuticals, Inc.",
    "SubstanceName": "REMIFENTANIL HYDROCHLORIDE",
    "StrengthNumber": "1",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Full Opioid Agonists [MoA], Opioid Agonist [EPC]",
    "DEASchedule": "CII",
    "Status": "Deprecated",
    "LastUpdate": "2026-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20240904",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}