81964-220-40 : NDC 2026 Code

81964-220-40 : Amoxicillin And Clavulanate Potassium ( Amoxicillin And Clavulanate Potassium )

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NDC Code : 81964-220-40 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "81964-220-40",
    "PackageDescription": "40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-40) ",
    "NDC11Code": "81964-0220-40",
    "ProductNDC": "81964-220",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amoxicillin And Clavulanate Potassium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amoxicillin And Clavulanate Potassium",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20251215",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA050785",
    "LabelerName": "USAntibiotics, LLC",
    "SubstanceName": "AMOXICILLIN; AMOXICILLIN SODIUM; CLAVULANATE POTASSIUM",
    "StrengthNumber": "562.5; 437.5; 62.5",
    "StrengthUnit": "mg/1; mg/1; mg/1",
    "Pharm_Classes": "Penicillin-class Antibacterial [EPC], Penicillin-class Antibacterial [EPC], Penicillins [CS], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-16",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20251215",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}