{
"NDC": {
"NDCCode": "60687-239-56",
"PackageDescription": "10 TRAY in 1 CASE (60687-239-56) > 10 CUP, UNIT-DOSE in 1 TRAY (60687-239-48) > 10 mL in 1 CUP, UNIT-DOSE (60687-239-42) ",
"NDC11Code": "60687-0239-56",
"ProductNDC": "60687-239",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Amantadine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Amantadine Hydrochloride",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20200831",
"EndMarketingDate": "20220531",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075060",
"LabelerName": "American Health Packaging",
"SubstanceName": "AMANTADINE HYDROCHLORIDE",
"StrengthNumber": "50",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Influenza A M2 Protein Inhibitor [EPC], M2 Protein Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-06-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20200831",
"EndMarketingDatePackage": "20220531",
"SamplePackage": "N"
}
}