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SafetyAlerts
August 8, 2000

Pannaz Tablets Recalled

Irvine, CA (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Anabolic Laboratories, Inc. is conducting a recall of Pannaz(tm) Tablets because there was a lack of complete manufacturing process validation.

PRODUCT
Pannaz(tm) Tablets, antihistamine-decongestant (Phenylpropanolamine HCl, 75 mg, Chlorpheniramine Maleate 8 mg, Methscopolamine Nitrate 2.5 mg), in 100-tablet bottles, Rx. NDC #0525-0780-01.

Recall #D-443-0.  Class III

CODE
Lot #V6337A01 EXP 5/02.

MANUFACTURER
Anabolic Laboratories, Inc., Irvine, California.

RECALLED BY
Manufacturer, by letter dated June 14, 2000. Firm-initiated recall ongoing.  This is the first public notice issued by the FDA.

DISTRIBUTION
Undetermined.

QUANTITY
9,493 bottles were distributed.

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 SafeMail subscribers August 8, 2000.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

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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.