FDA Overview (cont.)Medical Author:
Mitchell S Berger, MPH, JD
Coauthor:
Barry A Berger, JD, MBA
Medical Editor:
James E Keany, MD, FACEP
Medical Editor:
Francisco Talavera, PharmD, PhD
Medical Editor:
Jeter (Jay) Pritchard Taylor III, MD
IN THIS ARTICLEAuthors and EditorsAuthor: Mitchell S Berger, MPH, JD, Editor, FDA Enforcement Manual, FDA Group, Thompson Publishing Group.Coauthor(s): Barry A Berger, JD, MBA, Senior Counsel, GlaxoSmithKline. Editors: James E Keany, MD, FACEP, Director of Emergency Medical Education, Department of Emergency Medicine, Mission Hospital Regional Medical Center and Children's Hospital at Miss; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Jeter (Jay) Pritchard Taylor III, MD, Vice-Chief, Compliance Officer, Attending Physician Emergency Medicine Residency, Department of Emergency Medicine, Palmetto Richland Memorial Hospital, University of South Carolina. Last Editorial Review: 10/17/2005 |
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The FDA has approved first-time generic formulations for oxycodone hydrochloride and ibuprofen tablets in 5 mg/400 mg strength, extended phenytoin sodium capsules in 30-mg strength, and fomepizole injectable in 1 g/mL strength.
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