Published Jan 19, 2005
Brian, ASN, RN
3 Articles; 3,695 Posts
MedWatch - The FDA Safety Information and Adverse Event Reporting Program
FDA and Alliant Pharmaceuticals notified healthcare professionals and
consumers of the voluntary recall of one lot of Methylphenidate HCl Chewable
Tablets, 5 mg strength,indicated for Attention Deficit Hyperactivity
Disorder and Narcolepsy. After testing and evaluation, Alliant found that
lot number #AMT50402A [expiration date April 2006] might contain up to three
times the active ingredient, and elected to recall the medication as it
could pose serious health risk for some patients.
Read the MedWatch 2005 safety summary, including links to the Firm Press
Release, at:
http://www.fda.gov/medwatch/SAFETY/2005/safety05.htm#Methylin