0536-1491-34 : NDC 2026 Code

0536-1491-34 : Fexofenadine Hydrochloride, Pseudoephedrine Hydrochloride ( Rugby Allergy Relief D )

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NDC Code : 0536-1491-34 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0536-1491-34",
    "PackageDescription": "20 BLISTER PACK in 1 CARTON (0536-1491-34)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK",
    "NDC11Code": "00536-1491-34",
    "ProductNDC": "0536-1491",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Rugby Allergy Relief D",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine Hydrochloride, Pseudoephedrine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20260708",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216792",
    "LabelerName": "Rugby Laboratories",
    "SubstanceName": "FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE",
    "StrengthNumber": "60; 120",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-07-13",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260708",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}