63739-005-32 : NDC 2026 Code

63739-005-32 : Ziprasidone Hydrochloride ( Ziprasidone Hydrochloride )

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NDC Code : 63739-005-32 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-005-32",
    "PackageDescription": "4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32)  / 10 CAPSULE in 1 BLISTER PACK",
    "NDC11Code": "63739-0005-32",
    "ProductNDC": "63739-005",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ziprasidone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ziprasidone Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20120302",
    "EndMarketingDate": "20260331",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077565",
    "LabelerName": "McKesson Corporation dba SKY Packaging",
    "SubstanceName": "ZIPRASIDONE HYDROCHLORIDE",
    "StrengthNumber": "40",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Atypical Antipsychotic [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-01-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20160111",
    "EndMarketingDatePackage": "20260331",
    "SamplePackage": "N"
  }
}