70436-200-06 : NDC 2026 Code

70436-200-06 : Diltiazem Hydrochloride ( Diltiazem Hydrochloride )

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NDC Code : 70436-200-06 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70436-200-06",
    "PackageDescription": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-200-06) ",
    "NDC11Code": "70436-0200-06",
    "ProductNDC": "70436-200",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Diltiazem Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diltiazem Hydrochloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20230320",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216439",
    "LabelerName": "Slate Run Pharmaceuticals, LLC",
    "SubstanceName": "DILTIAZEM HYDROCHLORIDE",
    "StrengthNumber": "420",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20230320",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}