{
"NDC": {
"NDCCode": "61314-320-01",
"PackageDescription": "1 BOTTLE in 1 CARTON (61314-320-01) > 30500 uL in 1 BOTTLE",
"NDC11Code": "61314-0320-01",
"ProductNDC": "61314-320",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Olopatadine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Olopatadine Hydrochloride",
"DosageFormName": "SPRAY, METERED",
"RouteName": "NASAL",
"StartMarketingDate": "20150401",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA021861",
"LabelerName": "Sandoz Inc",
"SubstanceName": "OLOPATADINE HYDROCHLORIDE",
"StrengthNumber": "665",
"StrengthUnit": "ug/100uL",
"Pharm_Classes": "Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-10-27",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20150401",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}