60687-641-21 : NDC 2026 Code

60687-641-21 : Nebivolol ( Nebivolol )

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NDC Code : 60687-641-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-641-21",
    "PackageDescription": "30 BLISTER PACK in 1 CARTON (60687-641-21)  / 1 TABLET in 1 BLISTER PACK (60687-641-11) ",
    "NDC11Code": "60687-0641-21",
    "ProductNDC": "60687-641",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Nebivolol",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Nebivolol",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220907",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA203828",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "NEBIVOLOL HYDROCHLORIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-05-20",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220907",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}