{
"NDC": {
"NDCCode": "51672-4256-9",
"PackageDescription": "1 BOTTLE in 1 CARTON (51672-4256-9) / 340 mL in 1 BOTTLE",
"NDC11Code": "51672-4256-09",
"ProductNDC": "51672-4256",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Perampanel",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Perampanel",
"DosageFormName": "SUSPENSION",
"RouteName": "ORAL",
"StartMarketingDate": "20260616",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA219052",
"LabelerName": "Sun Pharmaceutical Industries, Inc.",
"SubstanceName": "PERAMPANEL",
"StrengthNumber": ".5",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "AMPA Receptor Antagonists [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Noncompetitive AMPA Glutamate Receptor Antagonist [EPC], UGT1A9 Inhibitors [MoA], UGT2B7 Inhibitors [MoA]",
"DEASchedule": "CIII",
"Status": "Active",
"LastUpdate": "2026-06-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260616",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}