70934-944-90 : NDC 2026 Code

70934-944-90 : Amlodipine Besylate And Benazepril Hydrochloride ( Amlodipine Besylate And Benazepril Hydrochloride )

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NDC Code : 70934-944-90 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70934-944-90",
    "PackageDescription": "90 CAPSULE in 1 BOTTLE, PLASTIC (70934-944-90) ",
    "NDC11Code": "70934-0944-90",
    "ProductNDC": "70934-944",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amlodipine Besylate And Benazepril Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amlodipine Besylate And Benazepril Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220203",
    "EndMarketingDate": "20240131",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077183",
    "LabelerName": "Denton Pharma, Inc. DBA Northwind Pharmaceuticals",
    "SubstanceName": "AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE",
    "StrengthNumber": "5; 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": "Deprecated",
    "LastUpdate": "2024-02-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20220203",
    "EndMarketingDatePackage": "20240131",
    "SamplePackage": "N"
  }
}