FOR IMMEDIATE RELEASE Contact: Evita Almassi, email@example.com or (202) 682-6240
What’s the difference between generic and brand-name prescription drugs?
Last week we attended a public meeting at the Food and Drug Administration (FDA) where we testified in front of supporters and opponents on behalf of the FDA’s proposed rule on Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products.
More than 80 percent of prescriptions filled in the United States are for generic drugs. Women get these prescriptions with the assumption that the drugs they’ve been prescribed are safe and effective.
Statement of Coco Jervis, J.D., Program Director |
Food and Drug Administration Public Meeting on Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products
FOR IMMEDIATE RELEASE
Contact: Coco Jervis 202.407.0788