{
"NDC": {
"NDCCode": "70518-3838-0",
"PackageDescription": "10 CUP in 1 BOX (70518-3838-0) / 5 mL in 1 CUP (70518-3838-1) ",
"NDC11Code": "70518-3838-00",
"ProductNDC": "70518-3838",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Fluoxetine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Fluoxetine Hydrochloride",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20180821",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA216448",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "FLUOXETINE HYDROCHLORIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-12-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20180821",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}