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53217-138-30 : NDC 2026 Code

53217-138-30 : Buprenorphine Hydrochloride And Naloxone Hydrochloride ( Buprenorphine And Naloxone )

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NDC Code : 53217-138-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "53217-138-30",
    "PackageDescription": "30 TABLET in 1 BOTTLE (53217-138-30)",
    "NDC11Code": "53217-0138-30",
    "ProductNDC": "53217-138",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Buprenorphine And Naloxone",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Buprenorphine Hydrochloride And Naloxone Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "SUBLINGUAL",
    "StartMarketingDate": "20151210",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA204431",
    "LabelerName": "Aidarex Pharmaceuticals LLC",
    "SubstanceName": "BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE",
    "StrengthNumber": "8; 2",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC],Opioid Antagonist [EPC],Opioid Antagonists [MoA]",
    "DEASchedule": "CIII",
    "Status": "Deprecated",
    "LastUpdate": "2020-01-01",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}
                
            

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