72819-149-07 : NDC 2026 Code

72819-149-07 : Nicardipine Hydrochloride ( Nicardipine Hydrochloride )

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NDC Code : 72819-149-07 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72819-149-07",
    "PackageDescription": "10 VIAL in 1 CARTON (72819-149-07)  / 10 mL in 1 VIAL (72819-149-06) ",
    "NDC11Code": "72819-0149-07",
    "ProductNDC": "72819-149",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Nicardipine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Nicardipine Hydrochloride",
    "DosageFormName": "INJECTION, SOLUTION",
    "RouteName": "INTRAVENOUS",
    "StartMarketingDate": "20241207",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090664",
    "LabelerName": "Archis Pharma LLC",
    "SubstanceName": "NICARDIPINE HYDROCHLORIDE",
    "StrengthNumber": "2.5",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Calcium Channel Antagonists [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-12-10",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20241207",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}