{
"NDC": {
"NDCCode": "60687-156-25",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-156-25) / 1 TABLET, CHEWABLE in 1 BLISTER PACK (60687-156-95) ",
"NDC11Code": "60687-0156-25",
"ProductNDC": "60687-156",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Phenytoin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Phenytoin",
"DosageFormName": "TABLET, CHEWABLE",
"RouteName": "ORAL",
"StartMarketingDate": "20151202",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA200565",
"LabelerName": "American Health Packaging",
"SubstanceName": "PHENYTOIN",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2024-10-10",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20151202",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}