{
"NDC": {
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"PackageDescription": "10 VIAL, SINGLE-DOSE in 1 CARTON (70860-407-10) / 10 mL in 1 VIAL, SINGLE-DOSE (70860-407-41) ",
"NDC11Code": "70860-0407-10",
"ProductNDC": "70860-407",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Tranexamic Acid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Tranexamic Acid",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20220922",
"EndMarketingDate": "20251231",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA203521",
"LabelerName": "Athenex Pharmaceutical Division, LLC.",
"SubstanceName": "TRANEXAMIC ACID",
"StrengthNumber": "100",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2026-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20220922",
"EndMarketingDatePackage": "20251231",
"SamplePackage": "N"
}
}