43063-349-15 : NDC 2026 Code

43063-349-15 : Hydrocodone Bitartrate And Ibuprofen ( Hydrocodone Bitartrate And Ibuprofen )

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NDC Code : 43063-349-15 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "43063-349-15",
    "PackageDescription": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-349-15) ",
    "NDC11Code": "43063-0349-15",
    "ProductNDC": "43063-349",
    "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": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076604",
    "LabelerName": "PD-Rx Pharmaceuticals, 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": "2018-09-25",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20170127",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}