63739-538-55 : NDC 2026 Code

63739-538-55 : Lactulose ( Lactulose )

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NDC Code : 63739-538-55 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-538-55",
    "PackageDescription": "2 TRAY in 1 CASE (63739-538-55)  &gt; 10 CUP, UNIT-DOSE in 1 TRAY &gt; 30 mL in 1 CUP, UNIT-DOSE",
    "NDC11Code": "63739-0538-55",
    "ProductNDC": "63739-538",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lactulose",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lactulose",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20111101",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075993",
    "LabelerName": "McKesson Packaging Services a business unit of McKesson Corporation",
    "SubstanceName": "LACTULOSE",
    "StrengthNumber": "10",
    "StrengthUnit": "g/15mL",
    "Pharm_Classes": "Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-04-18",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}