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Mebrofenin (AnazaoHealth Corporation)

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INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-216-01) Label Information

Complete Mebrofenin Information

  • SPL UNCLASSIFIED SECTION

    Dear Medical Professional,

    Per your order, we have compounded Mebrofenin as a sterile solution. The characteristics of this preparation are


  • DESCRIPTION

    AnazaoHealth supplies compounded Mebrofenin for the preparation of Tc-99m Mebrofenin. Each reaction vial contains 10 mg Mebrofenin and 0.2 mg tin as stannous chloride. The vial is back filled with nitrogen gas after lyophilization. The vial may contain a partial vacuum.


  • INDICATIONS AND USAGE

    Technetium Tc-99m Mebrofenin by intravenous administration is indicated as a hepatic imaging agent, used in the diagnosis of liver disease


  • DOSAGE AND ADMINISTRATION

    The suggested intravenous dose range of Technetium Tc 99m Mebrofenin in the average patient (70 kg) is:

    Nonjaundiced patient: 74 - 185 MBq (2-5 mCi)

    Patient with serum bilirubin level greater than 1.5 mg/dL: 111-370 MBq (3-10 mCi)

    The patient should be in a fasting state, 4 hours is preferable. False positives (non-visualization) may result if the gallbladder has been emptied by ingestion of food.

    An interval of at least 24 hours should be allowed before repeat examination


  • PREPARATION

    To prepare injection, follow this aseptic procedure:

    1. Waterproof gloves should be worn during the preparation procedure.
    2. Snap off the plastic lid and place room temperature reaction vial in an appropriate lead shield.
    3. Swab the rubber closure of the vial with a germicide.
    4. Inject 1 – 3 ml Sterile additive free sodium pertechnetate Tc-99m injection containing up to 740 MBq (20 mCi) into the vial. Be sure to maintain inert atmosphere in vial by introducing as little air as possible during reconstitution. NOTE: If sodium pertechnetate Tc-99m injection must be diluted, use only preservative free Sodium Chloride Injection USP.
    5. Secure the lead shield cover. Swirl the vial gently to mix contents and let stand 3 to 5 minutes prior to use.
    6. Record the date and time of preparation on a pressure-sensitive label.
    7. Affix pressure-sensitive label to shield.
    8. Examine vial contents; if the solution is not clear and free of particulate matter and discoloration on visual inspection, it should not be used.
    9. Measure the radioactivity by suitable calibration system and record prior to patient administration.
    10. Appropriate quality control is recommended.
    11. Use within 12 hours of preparation

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Figure 1

    C:\Users\achai\Desktop\NDC Project-AC 2012\Mebrofenin\Mebrolabel.JPG

  • INGREDIENTS AND APPEARANCE
    MEBROFENIN 
    mebrofenin injection, powder, lyophilized, for solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51808-216
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MEBROFENIN (UNII: 7PV0B6ED98) (MEBROFENIN - UNII:7PV0B6ED98) MEBROFENIN 10 mg
    Inactive Ingredients
    Ingredient Name Strength
    STANNOUS CHLORIDE (UNII: 1BQV3749L5) 0.2 mg
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51808-216-01 1 in 1 KIT
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved drug other 06/19/2012
    Labeler - AnazaoHealth Corporation (011038762)
    Establishment
    Name Address ID/FEI Business Operations
    AnazaoHealth Corporation 011038762 MANUFACTURE(51808-216)