Plaintiffs allege ranitidine, the active ingredient in Zantac and its generic equivalents, is unstable and breaks down into NDMA, a probable human carcinogen. Hundreds of personal injury suits alleging years of antacid use caused cancer, and proposed class suits seeking refunds, are proceeding in the U.S. District Court for the Southern District of Florida.
Federal drug labeling law bars design defect and failure-to-warn claims against generic ...
Learn more about Bloomberg Law or Log In to keep reading:
See Breaking News in Context
Bloomberg Law provides trusted coverage of current events enhanced with legal analysis.
Already a subscriber?
Log in to keep reading or access research tools and resources.