{
"NDC": {
"NDCCode": "33342-556-11",
"PackageDescription": "100 CAPSULE in 1 CONTAINER (33342-556-11) ",
"NDC11Code": "33342-0556-11",
"ProductNDC": "33342-556",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Mexiletine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Mexiletine Hydrochloride",
"DosageFormName": "CAPSULE",
"RouteName": "ORAL",
"StartMarketingDate": "20260323",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA219987",
"LabelerName": "Macleods Pharmaceuticals Limited",
"SubstanceName": "MEXILETINE HYDROCHLORIDE",
"StrengthNumber": "200",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antiarrhythmic [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-04-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260323",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}