59651-250-01 : NDC 2026 Code

59651-250-01 : Desmopressin Acetate ( Desmopressin Acetate )

Additionally :

You can get information about “59651-250-01” NDC code in 59651-250-01 in HTML format

HTML | 59651-250-01 in TXT (Plain Text) format

TXT | 59651-250-01 in PDF (Portable Document Format)

PDF | 59651-250-01 in XML format

XML formats.

NDC Code : 59651-250-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "59651-250-01",
    "PackageDescription": "100 TABLET in 1 BOTTLE (59651-250-01) ",
    "NDC11Code": "59651-0250-01",
    "ProductNDC": "59651-250",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Desmopressin Acetate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Desmopressin Acetate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240321",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA213095",
    "LabelerName": "Aurobindo Pharma Limited",
    "SubstanceName": "DESMOPRESSIN ACETATE",
    "StrengthNumber": ".2",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Factor VIII Activator [EPC], Increased Coagulation Factor VIII Activity [PE], Increased Coagulation Factor VIII Concentration [PE], Vasopressin Analog [EPC], Vasopressins [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-03-28",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20240321",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}