{
"NDC": {
"NDCCode": "63739-391-10",
"PackageDescription": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-391-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "63739-0391-10",
"ProductNDC": "63739-391",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Gabapentin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Gabapentin",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20040214",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075694",
"LabelerName": "McKesson Corporation",
"SubstanceName": "GABAPENTIN",
"StrengthNumber": "600",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-11-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20040214",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}