82012-029-04 : NDC 2026 Code

82012-029-04 : Mexiletine Hydrochloride ( Mexiletine Hydrochloride )

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NDC Code : 82012-029-04 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "82012-029-04",
    "PackageDescription": "100 CAPSULE in 1 BOTTLE (82012-029-04) ",
    "NDC11Code": "82012-0029-04",
    "ProductNDC": "82012-029",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Mexiletine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Mexiletine Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20211129",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA214089",
    "LabelerName": "Senores Pharmaceuticals, Inc.",
    "SubstanceName": "MEXILETINE HYDROCHLORIDE",
    "StrengthNumber": "250",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Antiarrhythmic [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2023-06-19",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20211129",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}