{
"NDC": {
"NDCCode": "52536-059-03",
"PackageDescription": "30 TABLET in 1 BOTTLE (52536-059-03) ",
"NDC11Code": "52536-0059-03",
"ProductNDC": "52536-059",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Amphetamine Sulfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Amphetamine Sulfate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20180329",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA200166",
"LabelerName": "Wilshire Pharmaceuticals, Inc.",
"SubstanceName": "AMPHETAMINE SULFATE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]",
"DEASchedule": "CII",
"Status": "Active",
"LastUpdate": "2026-01-29",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20210107",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}