80674-210-10 : NDC 2026 Code

80674-210-10 : Fosphenytoin Sodium ( Sesquient )

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NDC Code : 80674-210-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "80674-210-10",
    "PackageDescription": "10 VIAL, SINGLE-USE in 1 CARTON (80674-210-10)  / 10 mL in 1 VIAL, SINGLE-USE (80674-210-01) ",
    "NDC11Code": "80674-0210-10",
    "ProductNDC": "80674-210",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sesquient",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fosphenytoin Sodium",
    "DosageFormName": "INJECTION, SOLUTION",
    "RouteName": "INTRAVENOUS",
    "StartMarketingDate": "20210601",
    "EndMarketingDate": "20231231",
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA210864",
    "LabelerName": "Sedor Pharmaceuticals, LLC",
    "SubstanceName": "FOSPHENYTOIN SODIUM",
    "StrengthNumber": "500",
    "StrengthUnit": "mg/10mL",
    "Pharm_Classes": "Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-01-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20210601",
    "EndMarketingDatePackage": "20231231",
    "SamplePackage": "N"
  }
}