51655-365-52 : NDC 2026 Code

51655-365-52 : Divalproex Sodium ( Divalproex Sodium )

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NDC Code : 51655-365-52 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51655-365-52",
    "PackageDescription": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-365-52) ",
    "NDC11Code": "51655-0365-52",
    "ProductNDC": "51655-365",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Divalproex Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Divalproex Sodium",
    "DosageFormName": "TABLET, DELAYED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200529",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079163",
    "LabelerName": "Northwind Pharmaceuticals, LLC",
    "SubstanceName": "DIVALPROEX SODIUM",
    "StrengthNumber": "250",
    "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": "2026-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20200529",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}