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    December 23, 2009 Approval Letter - Engerix-B

    December 23, 2009

    Our STN:  BL 103239/5272

    GlaxoSmithKline Biologicals
    Attention:  Wendy A. Valinski
    2301 Renaissance Boulevard
    P.O. Box 61540                                                                     
    King of Prussia, PA 19406-2772

    Dear Ms. Valinski:

    We have approved your request to supplement your biologics license application for Hepatitis B Vaccine (Recombinant), Engerix-B®, to update the Package Insert to include the addition of text to visually inspect vials or syringes for cracks prior to administration. 

    Please submit all final printed labeling at the time of use and include implementation information on FDA Form 356h.  Please provide content of labeling in Structured Product Labeling format.

    All promotional claims must be consistent with and not contrary to approved labeling.  You should not make a comparative promotional claim or claim of superiority over other products unless you have substantial evidence or substantial clinical experience to support such claims [21 CFR 202.1(e)(6)].

    We will include information contained in the above-referenced supplement in your biologics license application file.  

    Sincerely yours,

    --signature--

    Wellington Sun, M.D.
    Director
    Division of Vaccines and Related Products Applications
    Office of Vaccines Research and Review
    Center for Biologics Evaluation and Research

    Attachment:  Approved Final Draft Labeling

     

    Contact FDA

    (800) 835-4709
    (301) 827-1800
    Consumer Affairs Branch (CBER)

    Division of Communication and Consumer Affairs

    Office of Communication, Outreach and Development

    Food and Drug Administration

    1401 Rockville Pike

    Suite 200N/HFM-47

    Rockville, MD 20852-1448
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