{
"NDC": {
"NDCCode": "0904-6423-04",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-6423-04) > 1 TABLET in 1 BLISTER PACK",
"NDC11Code": "00904-6423-04",
"ProductNDC": "0904-6423",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Modafinil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Modafinil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20130403",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076715",
"LabelerName": "Major Pharmaceuticals",
"SubstanceName": "MODAFINIL",
"StrengthNumber": "100",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Central Nervous System Stimulation [PE], Increased Sympathetic Activity [PE], Sympathomimetic-like Agent [EPC]",
"DEASchedule": "CIV",
"Status": "Deprecated",
"LastUpdate": "2024-09-11",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20241231",
"StartMarketingDatePackage": "20130403",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}