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U.S. Department of Health and Human Services

Vaccines, Blood & Biologics

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July 18, 2006 Approval Letter - ABBOTT PRISM HBsAg; ABBOTT PRISM HBsAg Confirmatory

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Public Health Service
Food and Drug Administration
1401 Rockville Pike
Rockville, MD 20852-1448

July 18, 2006

Our STN: BL 103766/0

Abbott Laboratories
Attn: Susan Sanborn
D-49C, AP6C/2
100 Abbott Park Road
Chicago, IL 60064

Dear Ms. Sanborn:

We have approved your biologics license application for Antibody to Hepatitis B Surface Antigen (Mouse Monoclonal IgM) and Antibody to Hepatitis B Surface Antigen (Human) effective this date. You are hereby authorized to introduce or deliver for introduction into interstate commerce, Antibody to Hepatitis B Surface Antigen (Mouse Monoclonal IgM) and Antibody to Hepatitis B Surface Antigen (Human) under your existing Department of Health and Human Services U.S. License No. 0043. Antibody to Hepatitis B Surface Antigen [ABBOTT PRISM HBsAg] is an in vitro chemiluminescent immunoassay (ChLIA) indicated for the qualitative detection of hepatitis B surface antigen (HBsAg) in human serum and plasma specimens. The ABBOTT PRISM HBsAg is intended to be used as a screening test for individual human donors, including volunteer donors of whole blood and blood components, and other living donors for the presence of HBsAg. It is also intended for use in testing blood and plasma to screen organ donors when specimens are obtained while the donor's heart is still beating, and in testing blood specimens to screen cadaveric (non-heart-beating) donors. It is not intended for use on cord blood specimens. ABBOTT PRISM HBsAg Confirmatory assay is an in vitro qualitative chemiluminescent (ChLIA) used to confirm the presence of hepatitis B surface antigen (HBsAg) in human serum and plasma by means of specific antibody neutralization. The ABBOTT PRISM HBsAg Confirmatory assay is intended for confirmation of samples found to be repeatedly reactive by the ABBOTT PRISM HBsAg assay.

Under this license, you are approved to manufacture Antibody to Hepatitis B Surface Antigen (Mouse Monoclonal IgM) and Antibody to Hepatitis B Surface Antigen (Human) prepared at your facility, 100 Abbott Park Road, Chicago, IL 60064, REGISTRATION NUMBER 1415939. You must label your product with the proper names: Antibody to Hepatitis B Surface Antigen (Mouse Monoclonal IgM) and Antibody to Hepatitis B Surface Antigen (Human), [ABBOTT PRISM HBsAg, ABBOTT PRISM HBsAg Confirmatory] that we have approved, and market it as approved in your license application.

The dating period for Antibody to Hepatitis B Surface Antigen (Mouse Monoclonal IgM) and Antibody to Hepatitis B Surface Antigen (Human) shall be 12 months from the date of manufacture when stored at 2-8oC. The expiration date for the packaged product, ABBOTT PRISM HBsAg, shall be dependent on the shortest expiration date of any kit component.

Please submit final container samples of the product and each kit component in final containers together with protocols showing results of all applicable tests. You may not distribute any lots of product until you receive a notification of release from the Director, Center for Biologics Evaluation and Research (CBER).

You must submit information to your biologics license application for our review and written approval under 21 CFR 601.12 for any changes in the manufacturing, testing, packaging or labeling of Antibody to Hepatitis B Surface Antigen (Mouse Monoclonal IgM) and Antibody to Hepatitis B Surface Antigen (Human), or in the manufacturing facilities.

You must submit reports of biological product deviations under 21 CFR 600.14. You promptly should identify and investigate all manufacturing deviations, including those associated with processing, testing, packing, labeling, storage, holding and distribution. If the deviation involves a distributed product, may affect the safety, purity, or potency of the product, and meets the other criteria in the regulation, you must submit a report on Form FDA-3486 to the Director, Office of Compliance and Biologics Quality, Center for Biologics Evaluation and Research, HFM-600, 1401 Rockville Pike, Rockville, MD 20852-1448.

Please submit all final printed labeling at the time of use and include implementation information on FDA Form 356h and FDA Form 2567 as appropriate. Please provide a PDF-format electronic copy as well as original paper copies (ten for circulars and five for other labels). In addition, you may wish to submit two draft copies of the proposed introductory advertising and promotional labeling with an FDA Form 2253 to the Center for Biologics Evaluation and Research, Advertising and Promotional Labeling Branch, HFM-602, 1401 Rockville Pike, Rockville, MD 20852-1448. Two copies of final printed advertising and promotional labeling should be submitted at the time of initial dissemination, accompanied by a FDA Form 2253.

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 submitted data to support such claims to us and had them approved.

Sincerely yours,

 

Jay S. Epstein, M.D.
Director
Office of Blood Research and Review
Center for Biologics Evaluation and Research

 

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