72789-502-90 : NDC 2026 Code

72789-502-90 : Amlodipine Besylate And Benazepril Hydrochloride ( Amlodipine Besylate And Benazepril Hydrochloride )

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NDC Code : 72789-502-90 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72789-502-90",
    "PackageDescription": "90 CAPSULE in 1 BOTTLE, PLASTIC (72789-502-90) ",
    "NDC11Code": "72789-0502-90",
    "ProductNDC": "72789-502",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amlodipine Besylate And Benazepril Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amlodipine Besylate And Benazepril Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20180801",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078466",
    "LabelerName": "PD-Rx Pharmaceuticals, Inc.",
    "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": "2025-05-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250507",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}