61919-752-30 : NDC 2026 Code

61919-752-30 : Meclizine Hydrochloride ( Meclizine Hydrochloride )

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NDC Code : 61919-752-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "61919-752-30",
    "PackageDescription": "30 TABLET in 1 BOTTLE (61919-752-30)",
    "NDC11Code": "61919-0752-30",
    "ProductNDC": "61919-752",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Meclizine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Meclizine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20150101",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA200294",
    "LabelerName": "DirectRX",
    "SubstanceName": "MECLIZINE HYDROCHLORIDE",
    "StrengthNumber": "25",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Antiemetic [EPC],Emesis Suppression [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-09-21",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}