83008-089-90 : NDC 2026 Code

83008-089-90 : Ibuprofen And Famotidine ( Ibuprofen And Famotidine )

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NDC Code : 83008-089-90 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "83008-089-90",
    "PackageDescription": "90 TABLET, FILM COATED in 1 BOTTLE (83008-089-90) ",
    "NDC11Code": "83008-0089-90",
    "ProductNDC": "83008-089",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ibuprofen And Famotidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ibuprofen And Famotidine",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240910",
    "EndMarketingDate": "20251031",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211890",
    "LabelerName": "Quality Care Products, LLC",
    "SubstanceName": "FAMOTIDINE; IBUPROFEN",
    "StrengthNumber": "26.6; 800",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-11-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20240910",
    "EndMarketingDatePackage": "20251031",
    "SamplePackage": "N"
  }
}