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    NDC 00049-0114-28 ERAXIS 50 mg/15mL Details

    ERAXIS 50 mg/15mL

    ERAXIS is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Roerig. The primary component is ANIDULAFUNGIN.

    Product Information

    NDC 00049-0114
    Product ID 0049-0114_fa6cff94-4d7e-4240-b7e1-7fd3e573ed47
    Associated GPIs 11500010002120
    GCN Sequence Number 060436
    GCN Sequence Number Description anidulafungin VIAL 50 MG INTRAVEN
    HIC3 W3A
    HIC3 Description ANTIFUNGAL ANTIBIOTICS
    GCN 26594
    HICL Sequence Number 033502
    HICL Sequence Number Description ANIDULAFUNGIN
    Brand/Generic Brand
    Proprietary Name ERAXIS
    Proprietary Name Suffix n/a
    Non-Proprietary Name anidulafungin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 50
    Active Ingredient Units mg/15mL
    Substance Name ANIDULAFUNGIN
    Labeler Name Roerig
    Pharmaceutical Class Echinocandin Antifungal [EPC], Lipopeptides [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021632
    Listing Certified Through 2024-12-31

    Package

    NDC 00049-0114-28 (00049011428)

    NDC Package Code 0049-0114-28
    Billing NDC 00049011428
    Package 15 mL in 1 VIAL, SINGLE-USE (0049-0114-28)
    Marketing Start Date 2006-02-17
    NDC Exclude Flag N
    Pricing Information N/A