{
"NDC": {
"NDCCode": "52125-984-19",
"PackageDescription": "90 TABLET in 1 BOTTLE (52125-984-19)",
"NDC11Code": "52125-0984-19",
"ProductNDC": "52125-984",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Gabapentin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Gabapentin",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20160408",
"EndMarketingDate": "20170526",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA202764",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "GABAPENTIN",
"StrengthNumber": "800",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-01-13",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}