{
"NDC": {
"NDCCode": "68084-737-01",
"PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-737-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-737-11) ",
"NDC11Code": "68084-0737-01",
"ProductNDC": "68084-737",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Citalopram",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Citalopram Hydrobromide",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20140318",
"EndMarketingDate": "20240930",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077031",
"LabelerName": "American Health Packaging",
"SubstanceName": "CITALOPRAM HYDROBROMIDE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-10-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20140318",
"EndMarketingDatePackage": "20240930",
"SamplePackage": "N"
}
}