0615-7521-39 : NDC 2026 Code

0615-7521-39 : Oxybutynin Chloride ( Oxybutynin Chloride )

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NDC Code : 0615-7521-39 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0615-7521-39",
    "PackageDescription": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7521-39)",
    "NDC11Code": "00615-7521-39",
    "ProductNDC": "0615-7521",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Oxybutynin Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Oxybutynin Chloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20070510",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA020897",
    "LabelerName": "NCS HealthCare of KY, Inc dba Vangard Labs",
    "SubstanceName": "OXYBUTYNIN CHLORIDE",
    "StrengthNumber": "15",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-09-21",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}