{
"NDC": {
"NDCCode": "60687-654-01",
"PackageDescription": "100 BLISTER PACK in 1 CARTON (60687-654-01) > 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (60687-654-11) ",
"NDC11Code": "60687-0654-01",
"ProductNDC": "60687-654",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Divalproex Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Divalproex Sodium",
"DosageFormName": "CAPSULE, COATED PELLETS",
"RouteName": "ORAL",
"StartMarketingDate": "20220628",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA213181",
"LabelerName": "American Health Packaging",
"SubstanceName": "DIVALPROEX SODIUM",
"StrengthNumber": "125",
"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": "2023-08-12",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20220628",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}