63739-517-10 : NDC 2026 Code

63739-517-10 : Lamotrigine ( Lamotrigine )

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NDC Code : 63739-517-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-517-10",
    "PackageDescription": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-517-10)  &gt; 10 TABLET in 1 BLISTER PACK",
    "NDC11Code": "63739-0517-10",
    "ProductNDC": "63739-517",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lamotrigine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lamotrigine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20110608",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090607",
    "LabelerName": "McKesson Corporation dba SKY Packaging",
    "SubstanceName": "LAMOTRIGINE",
    "StrengthNumber": "200",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Anti-epileptic Agent [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-07-14",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": "20110608",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}