{
"NDC": {
"NDCCode": "60429-273-05",
"PackageDescription": "500 TABLET in 1 BOTTLE (60429-273-05)",
"NDC11Code": "60429-0273-05",
"ProductNDC": "60429-273",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Primidone",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Primidone",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20060701",
"EndMarketingDate": "20150830",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040667",
"LabelerName": "Golden State Medical Supply, Inc.",
"SubstanceName": "PRIMIDONE",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2015-09-04",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}