{
"NDC": {
"NDCCode": "58118-1402-8",
"PackageDescription": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (58118-1402-8) ",
"NDC11Code": "58118-1402-08",
"ProductNDC": "58118-1402",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Phenytoin Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Phenytoin Sodium",
"DosageFormName": "CAPSULE, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20061212",
"EndMarketingDate": "20190901",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040621",
"LabelerName": "Clinical Solutions Wholesale",
"SubstanceName": "PHENYTOIN SODIUM",
"StrengthNumber": "100",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-09-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20061212",
"EndMarketingDatePackage": "20190901",
"SamplePackage": "N"
}
}