60687-109-21 : NDC 2026 Code

60687-109-21 : Desmopressin Acetate ( Desmopressin Acetate )

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NDC Code : 60687-109-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-109-21",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-109-21)  &gt; 1 TABLET in 1 BLISTER PACK (60687-109-11)",
    "NDC11Code": "60687-0109-21",
    "ProductNDC": "60687-109",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Desmopressin Acetate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Desmopressin Acetate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20151201",
    "EndMarketingDate": "20181130",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076470",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "DESMOPRESSIN ACETATE",
    "StrengthNumber": ".1",
    "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 [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2018-12-02",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}