70000-0602-1 : NDC 2026 Code

70000-0602-1 : Ibuprofen And Pseudoephedrine Hydrochloride ( Ibuprofen And Pseudoephedrine Hydrochloride )

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NDC Code : 70000-0602-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70000-0602-1",
    "PackageDescription": "40 TABLET in 1 BLISTER PACK (70000-0602-1) ",
    "NDC11Code": "70000-0602-01",
    "ProductNDC": "70000-0602",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Ibuprofen And Pseudoephedrine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ibuprofen And Pseudoephedrine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220523",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA074567",
    "LabelerName": "CARDINAL HEALTH 110, LLC DBA LEADER",
    "SubstanceName": "IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE",
    "StrengthNumber": "200; 30",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2022-06-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220523",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}