72578-214-16 : NDC 2026 Code

72578-214-16 : Ibuprofen And Famotidine ( Ibuprofen And Famotidine )

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NDC Code : 72578-214-16 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72578-214-16",
    "PackageDescription": "90 TABLET in 1 BOTTLE (72578-214-16) ",
    "NDC11Code": "72578-0214-16",
    "ProductNDC": "72578-214",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ibuprofen And Famotidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ibuprofen And Famotidine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250601",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA218684",
    "LabelerName": "Viona Pharmaceuticals Inc",
    "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": "Active",
    "LastUpdate": "2025-06-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250601",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}