{
"NDC": {
"NDCCode": "65302-062-05",
"PackageDescription": "6 POUCH in 1 CARTON (65302-062-05) > 5 AMPULE in 1 POUCH > .3 mL in 1 AMPULE",
"NDC11Code": "65302-0062-05",
"ProductNDC": "65302-062",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Tafluprost",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Tafluprost",
"DosageFormName": "SOLUTION",
"RouteName": "OPHTHALMIC",
"StartMarketingDate": "20221205",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA209040",
"LabelerName": "The Ritedose Corporation",
"SubstanceName": "TAFLUPROST",
"StrengthNumber": ".0045",
"StrengthUnit": "mg/.3mL",
"Pharm_Classes": "Increased Prostaglandin Activity [PE], Prostaglandin Analog [EPC], Prostaglandin Receptor Agonists [MoA], Prostaglandins [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-01-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20221205",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}