70934-280-30 : NDC 2026 Code

70934-280-30 : Amiodarone Hydrochloride ( Amiodarone Hydrochloride )

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NDC Code : 70934-280-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70934-280-30",
    "PackageDescription": "30 TABLET in 1 BOTTLE, PLASTIC (70934-280-30) ",
    "NDC11Code": "70934-0280-30",
    "ProductNDC": "70934-280",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Amiodarone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Amiodarone Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20190213",
    "EndMarketingDate": "20240531",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA204742",
    "LabelerName": "Denton Pharma, Inc. DBA Northwind Pharmaceuticals",
    "SubstanceName": "AMIODARONE HYDROCHLORIDE",
    "StrengthNumber": "200",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Antiarrhythmic [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-06-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20190213",
    "EndMarketingDatePackage": "20240531",
    "SamplePackage": "N"
  }
}