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    NDC 00409-1775-10 Dextrose 250 mg/mL Details

    Dextrose 250 mg/mL

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

    Product Information

    NDC 00409-1775
    Product ID 0409-1775_35a74bc2-fce3-46d2-a42d-645d19eb2e80
    Associated GPIs 80100020002030
    GCN Sequence Number 001992
    GCN Sequence Number Description dextrose 25 % in water SYRINGE 25 % INTRAVEN
    HIC3 C5J
    HIC3 Description IV SOLUTIONS: DEXTROSE-WATER
    GCN 06880
    HICL Sequence Number 000928
    HICL Sequence Number Description DEXTROSE 25 % 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 250
    Active Ingredient Units mg/mL
    Substance Name DEXTROSE MONOHYDRATE
    Labeler Name Hospira, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA019445
    Listing Certified Through 2025-12-31

    Package

    NDC 00409-1775-10 (00409177510)

    NDC Package Code 0409-1775-10
    Billing NDC 00409177510
    Package 10 CARTON in 1 PACKAGE (0409-1775-10) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0409-1775-40)
    Marketing Start Date 2006-02-22
    NDC Exclude Flag N
    Pricing Information N/A