51079-223-20 : NDC 2026 Code

51079-223-20 : Montelukast Sodium ( Montelukast Sodium )

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NDC Code : 51079-223-20 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-223-20",
    "PackageDescription": "100 BLISTER PACK in 1 CARTON (51079-223-20)  &gt; 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-223-01) ",
    "NDC11Code": "51079-0223-20",
    "ProductNDC": "51079-223",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Montelukast Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Montelukast Sodium",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20120828",
    "EndMarketingDate": "20190930",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079103",
    "LabelerName": "Mylan Institutional Inc.",
    "SubstanceName": "MONTELUKAST SODIUM",
    "StrengthNumber": "10",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-10-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20120828",
    "EndMarketingDatePackage": "20190930",
    "SamplePackage": "N"
  }
}