60687-148-21 : NDC 2026 Code

60687-148-21 : Oxymorphone Hydrochloride ( Oxymorphone Hydrochloride )

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NDC Code : 60687-148-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-148-21",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-148-21)  &gt; 1 TABLET in 1 BLISTER PACK (60687-148-11)",
    "NDC11Code": "60687-0148-21",
    "ProductNDC": "60687-148",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Oxymorphone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Oxymorphone Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20151201",
    "EndMarketingDate": "20180930",
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA021611",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "OXYMORPHONE HYDROCHLORIDE",
    "StrengthNumber": "10",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Full Opioid Agonists [MoA],Opioid Agonist [EPC]",
    "DEASchedule": "CII",
    "Status": "Deprecated",
    "LastUpdate": "2018-10-02",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}