{
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"PackageDescription": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 DOSE PACK (51079-723-63)",
"NDC11Code": "51079-0723-63",
"ProductNDC": "51079-723",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Oxybutynin Chloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Oxybutynin Chloride",
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"RouteName": "ORAL",
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"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076644",
"LabelerName": "UDL Laboratories, Inc.",
"SubstanceName": "OXYBUTYNIN CHLORIDE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]",
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"Status": "Deprecated",
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"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
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}
}