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FDA Clears for New Sprycel Product Labeling for Patients with Chronic-Phase CML
Bristol-Myers Squibb Company announced that the U.S. Food and Drug Administration (FDA) has approved new labeling for SPRYCEL to include a lower recom...

FDA Gives 510(k) Clearance to Baxter's New Antimicrobial Intravascular Technology
Baxter Healthcare Corporation announced that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its V-Link Luer-activat...

FDA-Approved Prescription Medications Now Available Online
As the political debate rages over the nuances of the American healthcare system, individuals are becoming more apprehensive about the prices of their...

15 Voting Members to Serve on FDA's Risk Communication Advisory Committee
The U.S. Food and Drug Administration has selected 15 voting members to serve on its Risk Communication Advisory Committee. The Committee will advise ...

Quality Associates Wins Major FDA Contract
Quality Associates, an established provider of services and solutions for document management, imaging and archiving, announced that it has been award...

Adams Respiratory Therapeutics Receives Approvable Letter From FDA for Mucinex(R) With Codeine
Adams Respiratory Therapeutics announced that the U.S. Food and Drug Administration (FDA) has issued an approvable letter related to the New Drug Appl...

Arrhythmia Research Technology Goes Live With IFS Applications Within Four Months
IFS, the global enterprise applications company, announced that Arrhythmia Research Technology has successfully gone live with IFS Applications in onl...

FDA Approves KV Pharmaceutical's Morphine ER 100 mg and 200 mg Tablets
KV Pharmaceutical Company announced that it has received approval from the U.S.Food and Drug Administration (FDA) on its application for the 100 mg an...

FDA Accepts Wyeth's Supplemental New Drug Application for Tygacil
Wyeth Pharmaceuticals, a division of Wyeth , announced that the U.S. Food and Drug Administration (FDA) has accepted for filing the Company's suppleme...

R7128 Receives Fast Track Designation from the FDA for the Treatment of Chronic Hepatitis C Infection
Pharmasset has received fast track designation from the U.S. Food and Drug Administration (FDA) for R7128 for the treatment of chronic hepatitis C vir...

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