57664-650-88 : NDC 2026 Code

57664-650-88 : Labetalol ( Labetalol )

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NDC Code : 57664-650-88 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "57664-650-88",
    "PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-650-88)",
    "NDC11Code": "57664-0650-88",
    "ProductNDC": "57664-650",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Labetalol",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Labetalol",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "19990729",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075215",
    "LabelerName": "Sun Pharmaceutical Industries, Inc.",
    "SubstanceName": "LABETALOL",
    "StrengthNumber": "100",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2018-04-25",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}