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    NDC 00517-6502-10 Selenious Acid 6 ug/mL Details

    Selenious Acid 6 ug/mL

    Selenious Acid is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by American Regent, Inc.. The primary component is SELENIUM.

    Product Information

    NDC 00517-6502
    Product ID 0517-6502_4f6657ea-8dfd-4a74-8a36-9855ca7fd34a
    Associated GPIs 79900040102003
    GCN Sequence Number 082958
    GCN Sequence Number Description selenium VIAL 6 MCG/ML INTRAVEN
    HIC3 C3M
    HIC3 Description MINERAL REPLACEMENT, MISCELLANEOUS
    GCN 51775
    HICL Sequence Number 000763
    HICL Sequence Number Description SELENIUM
    Brand/Generic Generic
    Proprietary Name Selenious Acid
    Proprietary Name Suffix n/a
    Non-Proprietary Name Selenious Acid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 6
    Active Ingredient Units ug/mL
    Substance Name SELENIUM
    Labeler Name American Regent, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA209379
    Listing Certified Through 2025-12-31

    Package

    NDC 00517-6502-10 (00517650210)

    NDC Package Code 0517-6502-10
    Billing NDC 00517650210
    Package 10 VIAL, SINGLE-DOSE in 1 BOX (0517-6502-10) / 2 mL in 1 VIAL, SINGLE-DOSE (0517-6502-01)
    Marketing Start Date 2022-03-28
    NDC Exclude Flag N
    Pricing Information N/A