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Voluntary recall issued for Nortrel 7/7/7 - 28 day.

Women's Health Weekly

| August 07, 2003 | COPYRIGHT 2003 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2003 AUG 7 - (NewsRx.com & NewsRx.net) -- Barr Laboratories, Inc., (BRL) announced that it is initiating a voluntary recall of three lots of its Nortrel 7/7/7 - 28 day (norethindrone and ethinyl estradiol tablets, USP) oral contraceptive product to the pharmacy level and is encouraging women who are currently taking the product to carefully examine their blister cards to confirm that the color-coded tablets are packaged in the proper color sequence.

The first three rows (labeled Start, Week 2, and Week 3) of a properly packaged product contain colored tablets. The last row (labeled Week 4) of a properly packaged product contains white tablets. The recall is being implemented because two ...

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