{
"NDC": {
"NDCCode": "50742-652-01",
"PackageDescription": "100 TABLET in 1 BOTTLE (50742-652-01) ",
"NDC11Code": "50742-0652-01",
"ProductNDC": "50742-652",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Amphetamine Sulfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Amphetamine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20200824",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA213763",
"LabelerName": "Ingenus Pharmaceuticals, LLC",
"SubstanceName": "AMPHETAMINE SULFATE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]",
"DEASchedule": "CII",
"Status": "Deprecated",
"LastUpdate": "2021-12-18",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20200824",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}