0115-6922-19 : NDC 2026 Code

0115-6922-19 : Divalproex Sodium ( Divalproex Sodium )

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NDC Code : 0115-6922-19 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0115-6922-19",
    "PackageDescription": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6922-19)",
    "NDC11Code": "00115-6922-19",
    "ProductNDC": "0115-6922",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Divalproex Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Divalproex Sodium",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20090804",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078791",
    "LabelerName": "Global Pharmaceuticals, Division of Impax Laboratories Inc.",
    "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": "2016-03-04",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}