43063-232-60 : NDC 2026 Code

43063-232-60 : Amlodipine Besylate And Benazepril Hydrochloride ( Amlodipine Besylate And Benazepril Hydrochloride )

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NDC Code : 43063-232-60 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "43063-232-60",
    "PackageDescription": "60 CAPSULE in 1 BOTTLE, PLASTIC (43063-232-60)",
    "NDC11Code": "43063-0232-60",
    "ProductNDC": "43063-232",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amlodipine Besylate And Benazepril Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amlodipine Besylate And Benazepril Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "19950303",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA020364",
    "LabelerName": "PD-Rx Pharmaceuticals, Inc.",
    "SubstanceName": "AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE",
    "StrengthNumber": "10; 20",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-10-23",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}