16590-815-82 : NDC 2025 Code

16590-815-82 : Phenytoin Sodium ( Phenytoin )

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NDC Code : 16590-815-82 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "16590-815-82",
    "PackageDescription": "180 CAPSULE in 1 BOTTLE, PLASTIC (16590-815-82)",
    "NDC11Code": "16590-0815-82",
    "ProductNDC": "16590-815",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Phenytoin",
    "ProprietaryNameSuffix": "Er",
    "NonProprietaryName": "Phenytoin Sodium",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20091120",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA040298",
    "LabelerName": "STAT RX USA LLC",
    "SubstanceName": "PHENYTOIN SODIUM",
    "StrengthNumber": "100",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2018-02-07",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}