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September 3, 2009 The U.S. Food and Drug Administration approved Intuniv, an extended release formulation of guanfacin as a pediatric treatment for attention deficit/hyperactivity disorder (ADHD). Clinical trials found the medication was better than a placebo at relieving ADHD symptoms for 24 hours. The medication, in dosage strengths of 1 mg, 2 mg, 3 mg, and 4 mg, will be available as of November 2009. Download the Report . . .

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Market Intelligence Resource | September 3, 2009

FDA NDA Approval Letter to Shire PLC for ADHD Medication Intuniv

September 3, 2009 The U.S. Food and Drug Administration approved Intuniv, an extended release formulation of guanfacin as a pediatric treatment for attention deficit/hyperactivity disorder (ADHD). Clinical trials found the medication was better than a placebo at relieving ADHD symptoms for 24 hours. The medication, in dosage strengths of 1 mg, 2 mg, 3 mg, and 4 mg, will be available as of November 2009. Download the Report . . .

Want To Read More? Log In Or Become A Paid Member
Resource Available For Paid OPEN MINDS Circle Members Only
Not a paid member? Don't miss out! Sign up today and receive unlimited organizational access to all OPEN MINDS strategic advice, market intelligence, and management best practices – over 250,000 resources!
Log In
If you are already a paid member, log in to your account to access this resource and more. If you are a free member, you will need to upgrade to a paid membership before accessing this resource.

Become A Paid Member
If you are not yet a paid member, learn more about the OPEN MINDS Circle Market Intelligence Service Membership on our website, reach out to our team at info@openminds.com, or call us at 877-350-6463.