{
"NDC": {
"NDCCode": "69315-503-24",
"PackageDescription": "236.5 mL in 1 BOTTLE (69315-503-24) ",
"NDC11Code": "69315-0503-24",
"ProductNDC": "69315-503",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Aminocaproic Acid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Aminocaproic Acid",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20210318",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA214140",
"LabelerName": "Leading Pharma, LLC",
"SubstanceName": "AMINOCAPROIC ACID",
"StrengthNumber": ".25",
"StrengthUnit": "g/mL",
"Pharm_Classes": "Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-01-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20210318",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}