{
"NDC": {
"NDCCode": "68180-521-50",
"PackageDescription": "50 POWDER, FOR SOLUTION in 1 CARTON (68180-521-50) ",
"NDC11Code": "68180-0521-50",
"ProductNDC": "68180-521",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Vigabatrin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Vigabatrin",
"DosageFormName": "POWDER, FOR SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20220310",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA211790",
"LabelerName": "Lupin Pharmaceuticals, Inc.",
"SubstanceName": "VIGABATRIN",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-10-18",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20220310",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}