31722-887-32 : NDC 2026 Code

31722-887-32 : Olmesartan Medoxomil And Hydrochlorothiazide ( Olmesartan Medoxomil And Hydrochlorothiazide )

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NDC Code : 31722-887-32 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "31722-887-32",
    "PackageDescription": "10 BLISTER PACK in 1 CARTON (31722-887-32)  / 10 TABLET, FILM COATED in 1 BLISTER PACK",
    "NDC11Code": "31722-0887-32",
    "ProductNDC": "31722-887",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Olmesartan Medoxomil And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Olmesartan Medoxomil And Hydrochlorothiazide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250725",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA209199",
    "LabelerName": "Camber Pharmaceuticals, Inc.",
    "SubstanceName": "HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL",
    "StrengthNumber": "12.5; 40",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-08-28",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250725",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}