45865-935-30 : NDC 2025 Code

45865-935-30 : Amlodipine And Olmesartan Medoxomil ( Amlodipine And Olmesartan Medoxomil )

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NDC Code : 45865-935-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "45865-935-30",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (45865-935-30) ",
    "NDC11Code": "45865-0935-30",
    "ProductNDC": "45865-935",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amlodipine And Olmesartan Medoxomil",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amlodipine And Olmesartan Medoxomil",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170815",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA207807",
    "LabelerName": "medsource pharmaceuticals",
    "SubstanceName": "AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL",
    "StrengthNumber": "5; 40",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20241231",
    "StartMarketingDatePackage": "20180601",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}