63629-7070-1 : NDC 2026 Code

63629-7070-1 : Labetalol Hydrochloride ( Labetalol Hydrochloride )

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NDC Code : 63629-7070-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63629-7070-1",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (63629-7070-1)",
    "NDC11Code": "63629-7070-01",
    "ProductNDC": "63629-7070",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Labetalol Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Labetalol Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "19980803",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075133",
    "LabelerName": "Bryant Ranch Prepack",
    "SubstanceName": "LABETALOL HYDROCHLORIDE",
    "StrengthNumber": "100",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-09-19",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}