71839-120-01 : NDC 2026 Code

71839-120-01 : Sodium Nitroprusside ( Sodium Nitroprusside )

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NDC Code : 71839-120-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "71839-120-01",
    "PackageDescription": "1 VIAL in 1 CARTON (71839-120-01)  &gt; 2 mL in 1 VIAL",
    "NDC11Code": "71839-0120-01",
    "ProductNDC": "71839-120",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sodium Nitroprusside",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Sodium Nitroprusside",
    "DosageFormName": "INJECTION",
    "RouteName": "INTRAVENOUS",
    "StartMarketingDate": "20210712",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA214971",
    "LabelerName": "BE Pharmaceuticals Inc.",
    "SubstanceName": "SODIUM NITROPRUSSIDE",
    "StrengthNumber": "50",
    "StrengthUnit": "mg/2mL",
    "Pharm_Classes": "Vasodilation [PE], Vasodilator [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2021-07-24",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20210712",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}