70518-2301-0 : NDC 2026 Code

70518-2301-0 : Ceftriaxone Sodium ( Ceftriaxone Sodium )

Additionally :

You can get information about “70518-2301-0” NDC code in 70518-2301-0 in HTML format

HTML | 70518-2301-0 in TXT (Plain Text) format

TXT | 70518-2301-0 in PDF (Portable Document Format)

PDF | 70518-2301-0 in XML format

XML formats.

NDC Code : 70518-2301-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-2301-0",
    "PackageDescription": "10 VIAL, SINGLE-USE in 1 CARTON (70518-2301-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2301-1) ",
    "NDC11Code": "70518-2301-00",
    "ProductNDC": "70518-2301",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ceftriaxone Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ceftriaxone Sodium",
    "DosageFormName": "INJECTION, POWDER, FOR SOLUTION",
    "RouteName": "INTRAMUSCULAR; INTRAVENOUS",
    "StartMarketingDate": "20190904",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA065169",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "CEFTRIAXONE SODIUM",
    "StrengthNumber": "500",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Cephalosporin Antibacterial [EPC], Cephalosporins [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-08-25",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20190904",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}