60687-717-01 : NDC 2026 Code

60687-717-01 : Diltiazem Hydrochloride ( Diltiazem Hydrochloride )

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NDC Code : 60687-717-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-717-01",
    "PackageDescription": "100 BLISTER PACK in 1 CARTON (60687-717-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-717-11) ",
    "NDC11Code": "60687-0717-01",
    "ProductNDC": "60687-717",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Diltiazem Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diltiazem Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20230327",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA074185",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "DILTIAZEM HYDROCHLORIDE",
    "StrengthNumber": "30",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-11-14",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20230327",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}