76237-108-30 : NDC 2025 Code

76237-108-30 : Amiodarone Hydrochloride ( Amiodarone Hydrochloride )

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NDC Code : 76237-108-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "76237-108-30",
    "PackageDescription": "6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-108-30)  &gt; 5 TABLET in 1 BLISTER PACK",
    "NDC11Code": "76237-0108-30",
    "ProductNDC": "76237-108",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amiodarone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amiodarone Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20120103",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075315",
    "LabelerName": "McKesson Contract Packaging",
    "SubstanceName": "AMIODARONE HYDROCHLORIDE",
    "StrengthNumber": "200",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Antiarrhythmic [EPC],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 1A2 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2018-03-07",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}