72189-260-90 : NDC 2026 Code

72189-260-90 : Amlodipine And Benazepril Hydrochloride ( Amlodipine And Benazepril Hydrochloride )

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NDC Code : 72189-260-90 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72189-260-90",
    "PackageDescription": "90 CAPSULE in 1 BOTTLE (72189-260-90) ",
    "NDC11Code": "72189-0260-90",
    "ProductNDC": "72189-260",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amlodipine And Benazepril Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amlodipine And Benazepril Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20210810",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA202239",
    "LabelerName": "DIRECT RX",
    "SubstanceName": "AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE",
    "StrengthNumber": "10; 20",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-01-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20210810",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}