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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.

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

Lot #V6337A01 EXP 5/02.

Anabolic Laboratories, Inc., Irvine, California.

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


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!

How many did you hear about?

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