48792-7894-1 : NDC 2026 Code

48792-7894-1 : Ranolazine ( Ranolazine )

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NDC Code : 48792-7894-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "48792-7894-1",
    "PackageDescription": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (48792-7894-1) ",
    "NDC11Code": "48792-7894-01",
    "ProductNDC": "48792-7894",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ranolazine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ranolazine",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200331",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211865",
    "LabelerName": "Sunshine Lake Pharma Co., Ltd.",
    "SubstanceName": "RANOLAZINE",
    "StrengthNumber": "1000",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Anti-anginal [EPC],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Organic Cation Transporter 2 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2021-11-10",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20221231",
    "StartMarketingDatePackage": "20200331",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}