{
"NDC": {
"NDCCode": "69452-227-20",
"PackageDescription": "100 TABLET in 1 BOTTLE (69452-227-20) ",
"NDC11Code": "69452-0227-20",
"ProductNDC": "69452-227",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Amphetamine Sulfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Amphetamine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20200115",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA212919",
"LabelerName": "Bionpharma Inc.",
"SubstanceName": "AMPHETAMINE SULFATE",
"StrengthNumber": "5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]",
"DEASchedule": "CII",
"Status": "Deprecated",
"LastUpdate": "2025-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20241231",
"StartMarketingDatePackage": "20200115",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}