0904-7079-57 : NDC 2026 Code

0904-7079-57 : Phenytoin ( Phenytoin )

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NDC Code : 0904-7079-57 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0904-7079-57",
    "PackageDescription": "50 CUP, UNIT-DOSE in 1 CASE (0904-7079-57)  &gt; 4 mL in 1 CUP, UNIT-DOSE (0904-7079-24) ",
    "NDC11Code": "00904-7079-57",
    "ProductNDC": "0904-7079",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Phenytoin",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Phenytoin",
    "DosageFormName": "SUSPENSION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20040408",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA040521",
    "LabelerName": "Major Pharmaceuticals",
    "SubstanceName": "PHENYTOIN",
    "StrengthNumber": "100",
    "StrengthUnit": "mg/4mL",
    "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": "2024-08-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20241231",
    "StartMarketingDatePackage": "20040408",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}