GENERIC NAME: bromfenac
BRAND NAME: Duract
IMPORTANT NEWS ALERT - The U.S. Food and Drug Administration (FDA) ordered the removal of bromfenac (DURACT) from the market in the United States because of potentially serious side effects.
Reference: FDA Prescribing Information
Quick GuidePrescription Drug Abuse Pictures Slideshow: Statistics, Facts, and Symptoms
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Need help identifying pills and medications?
Use the pill identifier tool on RxList.