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    NDC 55150-0222-20 ETOMIDATE 40 mg/20mL Details

    ETOMIDATE 40 mg/20mL

    ETOMIDATE is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eugia US LLC. The primary component is ETOMIDATE.

    Product Information

    NDC 55150-0222
    Product ID 55150-222_278b160e-cdc4-451e-9405-cb001f443680
    Associated GPIs 70400010002020
    GCN Sequence Number 030871
    GCN Sequence Number Description etomidate VIAL 2 MG/ML INTRAVEN
    HIC3 H2C
    HIC3 Description GENERAL ANESTHETICS,INJECTABLE
    GCN 12831
    HICL Sequence Number 001554
    HICL Sequence Number Description ETOMIDATE
    Brand/Generic Generic
    Proprietary Name ETOMIDATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name ETOMIDATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 40
    Active Ingredient Units mg/20mL
    Substance Name ETOMIDATE
    Labeler Name Eugia US LLC
    Pharmaceutical Class General Anesthesia [PE], General Anesthetic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206126
    Listing Certified Through 2024-12-31

    Package

    NDC 55150-0222-20 (55150022220)

    NDC Package Code 55150-222-20
    Billing NDC 55150022220
    Package 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-222-20) / 20 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2017-02-24
    NDC Exclude Flag N
    Pricing Information N/A