43068-610-09 : NDC 2026 Code

43068-610-09 : Ponesimod ( Ponvory )

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NDC Code : 43068-610-09 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "43068-610-09",
    "PackageDescription": "1 KIT in 1 CARTON (43068-610-09)  *  1 BLISTER PACK in 1 CARTON (43068-606-00)  / 1 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-609-00)  / 1 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-608-00)  / 1 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-607-00)  / 1 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-611-00)  / 3 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-605-00)  / 1 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-604-00)  / 2 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-603-00)  / 2 TABLET, FILM COATED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON (43068-602-00)  / 2 TABLET, FILM COATED in 1 BLISTER PACK",
    "NDC11Code": "43068-0610-09",
    "ProductNDC": "43068-610",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ponvory",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ponesimod",
    "DosageFormName": "KIT",
    "RouteName": null,
    "StartMarketingDate": "20210318",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA213498",
    "LabelerName": "Vanda Pharmaceuticals Inc.",
    "SubstanceName": null,
    "StrengthNumber": null,
    "StrengthUnit": null,
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-16",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20241101",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}