62037-524-05 : NDC 2026 Code

62037-524-05 : Hydrocodone Bitartrate And Ibuprofen ( Hydrocodone Bitartrate And Ibuprofen )

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NDC Code : 62037-524-05 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "62037-524-05",
    "PackageDescription": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62037-524-05) ",
    "NDC11Code": "62037-0524-05",
    "ProductNDC": "62037-524",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Hydrocodone Bitartrate And Ibuprofen",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Hydrocodone Bitartrate And Ibuprofen",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20040401",
    "EndMarketingDate": "20190930",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076604",
    "LabelerName": "Actavis Pharma, Inc.",
    "SubstanceName": "HYDROCODONE BITARTRATE; IBUPROFEN",
    "StrengthNumber": "7.5; 200",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]",
    "DEASchedule": "CII",
    "Status": "Deprecated",
    "LastUpdate": "2019-06-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20040401",
    "EndMarketingDatePackage": "20190531",
    "SamplePackage": "N"
  }
}