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    NDC 00338-9051-12 Micafungin in Sodium Chloride 50 mg/50mL Details

    Micafungin in Sodium Chloride 50 mg/50mL

    Micafungin in Sodium Chloride is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is MICAFUNGIN SODIUM.

    Product Information

    NDC 00338-9051
    Product ID 0338-9051_a95f901e-0ac4-4ec0-9720-9c6a066cd06c
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Micafungin in Sodium Chloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Micafungin in Sodium Chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAVENOUS
    Active Ingredient Strength 50
    Active Ingredient Units mg/50mL
    Substance Name MICAFUNGIN SODIUM
    Labeler Name Baxter Healthcare Corporation
    Pharmaceutical Class Echinocandin Antifungal [EPC], Lipopeptides [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA216142
    Listing Certified Through 2024-12-31

    Package

    NDC 00338-9051-12 (00338905112)

    NDC Package Code 0338-9051-12
    Billing NDC 00338905112
    Package 12 CARTON in 1 CARTON (0338-9051-12) / 1 BAG in 1 CARTON (0338-9051-01) / 50 mL in 1 BAG
    Marketing Start Date 2023-09-29
    NDC Exclude Flag N
    Pricing Information N/A