{
"NDC": {
"NDCCode": "17856-0109-1",
"PackageDescription": "100 POUCH in 1 BOX (17856-0109-1) / 1 CAPSULE, COATED PELLETS in 1 POUCH",
"NDC11Code": "17856-0109-01",
"ProductNDC": "17856-0109",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Divalproex Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Divalproex Sodium",
"DosageFormName": "CAPSULE, COATED PELLETS",
"RouteName": "ORAL",
"StartMarketingDate": "20190131",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078919",
"LabelerName": "ATLANTIC BIOLOGICALS CORP.",
"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": "Active",
"LastUpdate": "2025-06-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20210128",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}