{
"NDC": {
"NDCCode": "70377-089-01",
"PackageDescription": "50 PACKET in 1 CARTON (70377-089-01) > 10 mL in 1 PACKET",
"NDC11Code": "70377-0089-01",
"ProductNDC": "70377-089",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Vigabatrin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Vigabatrin",
"DosageFormName": "POWDER, FOR SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20220829",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA213390",
"LabelerName": "Biocon Pharma Inc.",
"SubstanceName": "VIGABATRIN",
"StrengthNumber": "500",
"StrengthUnit": "mg/10mL",
"Pharm_Classes": "Anti-epileptic Agent [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20241231",
"StartMarketingDatePackage": "20220829",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}