43063-402-60 : NDC 2026 Code

43063-402-60 : Amlodipine And Benazepril Hydrochloride ( Amlodipine And Benazepril Hydrochloride )

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NDC Code : 43063-402-60 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "43063-402-60",
    "PackageDescription": "60 CAPSULE in 1 BOTTLE, PLASTIC (43063-402-60) ",
    "NDC11Code": "43063-0402-60",
    "ProductNDC": "43063-402",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amlodipine And Benazepril Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amlodipine And Benazepril Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20070518",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077179",
    "LabelerName": "PD-Rx Pharmaceuticals, Inc.",
    "SubstanceName": "AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE",
    "StrengthNumber": "5; 20",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-09-24",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20121113",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}