63629-5687-4 : NDC 2026 Code

63629-5687-4 : Alfuzosin Hydrochloride ( Alfuzosin Hydrochloride )

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NDC Code : 63629-5687-4 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63629-5687-4",
    "PackageDescription": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5687-4)",
    "NDC11Code": "63629-5687-04",
    "ProductNDC": "63629-5687",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Alfuzosin Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Alfuzosin Hydrochloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20111122",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079057",
    "LabelerName": "Bryant Ranch Prepack",
    "SubstanceName": "ALFUZOSIN HYDROCHLORIDE",
    "StrengthNumber": "10",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-06-08",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}