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July 26, 2001

Vintage Pharmaceuticals Inc. Recalls Q Tuss Tablets

Charlotte, NC (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Vintage Pharmaceuticals, Inc. is recalling certain lot(s) of Q Tuss Tablets because of super-Potency (Scopolamine).

This is the first public notice of this Class II recall issued by FDA.

Q Tuss Tablets in bottles of 100's and 500's. The product is under the Zenith Goldline, URL, QT, VPI and URL label.

Lots - 010079A, 010079B, 010079C, 097089A, 098089A, 098089B, 098089C, 098089D, 098089E, 098089F, 099089A, 099089B, 136039A, 136039B, 136039C, 136039D, 008119A, 010119A, 011119A, 011119B, 011119C, 011119D, 011119E, 011119F, 009119A, 009119B, 009119C, 009119D, 009119E, 009119F, 011079A, 011079B, 011079C, 011079D, 011079E, 013090A, 013090B, 013090C, 100020C, 100020D, 012090A, 012090B

Recall Number: D-251-1

Vintage Pharmaceuticals, Charlotte, NC

Vintage by letter on 3/21/01



Q-Tuss Tablets - 110,538 bottles

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

Notice of this product warning was sent via email to SafetyAlerts subscribers July 26, 2001.  For more information regarding the SafetyAlerts free email alert service please click here.

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.