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    NDC 63323-0624-10 Dextrose 50 mg/mL Details

    Dextrose 50 mg/mL

    Dextrose is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Fresenius Kabi USA, LLC. The primary component is DEXTROSE MONOHYDRATE.

    Product Information

    NDC 63323-0624
    Product ID 63323-624_4cfbe8ac-5e60-4fa2-b96c-4206a098d555
    Associated GPIs 80100020002015
    GCN Sequence Number 001972
    GCN Sequence Number Description dextrose 5 % in water IV SOLN 5 % INTRAVEN
    HIC3 C5J
    HIC3 Description IV SOLUTIONS: DEXTROSE-WATER
    GCN 06641
    HICL Sequence Number 000915
    HICL Sequence Number Description DEXTROSE 5 % IN WATER
    Brand/Generic Generic
    Proprietary Name Dextrose
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dextrose Monohydrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 50
    Active Ingredient Units mg/mL
    Substance Name DEXTROSE MONOHYDRATE
    Labeler Name Fresenius Kabi USA, LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207449
    Listing Certified Through 2024-12-31

    Package

    NDC 63323-0624-10 (63323062410)

    NDC Package Code 63323-624-10
    Billing NDC 63323062410
    Package 10 BAG in 1 CASE (63323-624-10) / 1000 mL in 1 BAG (63323-624-03)
    Marketing Start Date 2016-10-21
    NDC Exclude Flag N
    Pricing Information N/A