{
"NDC": {
"NDCCode": "70518-1357-1",
"PackageDescription": "100 POUCH in 1 BOX (70518-1357-1) / 1 TABLET in 1 POUCH (70518-1357-2) ",
"NDC11Code": "70518-1357-01",
"ProductNDC": "70518-1357",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Citalopram Hydrobromide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Citalopram Hydrobromide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20180808",
"EndMarketingDate": "20250809",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078216",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "CITALOPRAM HYDROBROMIDE",
"StrengthNumber": "40",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-08-11",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20210217",
"EndMarketingDatePackage": "20250809",
"SamplePackage": "N"
}
}