63739-548-33 : NDC 2026 Code

63739-548-33 : Oxybutynin Chloride ( Oxybutynin Chloride )

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NDC Code : 63739-548-33 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-548-33",
    "PackageDescription": "3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-548-33)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK",
    "NDC11Code": "63739-0548-33",
    "ProductNDC": "63739-548",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Oxybutynin Chloride",
    "ProprietaryNameSuffix": "Extended Release",
    "NonProprietaryName": "Oxybutynin Chloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20090301",
    "EndMarketingDate": "20251130",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078503",
    "LabelerName": "McKesson Corporation dba SKY Packaging",
    "SubstanceName": "OXYBUTYNIN CHLORIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-12-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20090301",
    "EndMarketingDatePackage": "20251130",
    "SamplePackage": "N"
  }
}