{
"NDC": {
"NDCCode": "68084-317-01",
"PackageDescription": "10 BLISTER PACK in 1 CARTON (68084-317-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-317-11)",
"NDC11Code": "68084-0317-01",
"ProductNDC": "68084-317",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Divalproex Sodium Extended-release",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Divalproex Sodium Extended-release",
"DosageFormName": "TABLET, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20091014",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078705",
"LabelerName": "American Health Packaging",
"SubstanceName": "DIVALPROEX SODIUM",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2015-11-18",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}