63739-557-10 : NDC 2026 Code

63739-557-10 : Hydrocodone Bitartrate And Ibuprofen ( Hydrocodone Bitartrate And Ibuprofen )

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NDC Code : 63739-557-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-557-10",
    "PackageDescription": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-557-10)  &gt; 10 TABLET in 1 BLISTER PACK",
    "NDC11Code": "63739-0557-10",
    "ProductNDC": "63739-557",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Hydrocodone Bitartrate And Ibuprofen",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Hydrocodone Bitartrate And Ibuprofen",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20120521",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076642",
    "LabelerName": "McKesson Packaging Services a business unit of McKesson Corporation",
    "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": "CIII",
    "Status": "Deprecated",
    "LastUpdate": "2017-04-11",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}