51655-087-52 : NDC 2026 Code

51655-087-52 : Alfuzosin Hydrochloride ( Alfuzosin Hydrochloride )

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NDC Code : 51655-087-52 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51655-087-52",
    "PackageDescription": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52) ",
    "NDC11Code": "51655-0087-52",
    "ProductNDC": "51655-087",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Alfuzosin Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Alfuzosin Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20221004",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079060",
    "LabelerName": "Northwind Health Company, LLC",
    "SubstanceName": "ALFUZOSIN HYDROCHLORIDE",
    "StrengthNumber": "10",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-01-17",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20221004",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}