Pharma Closes in 71d
Zantac (Ranitidine) Master Settlement Fund
vs. GlaxoSmithKline / Sanofi / Boehringer Ingelheim
Master class for U.S. consumers who purchased over-the-counter Zantac or generic ranitidine between 2000-2020, where the active ingredient was later linked to NDMA contamination.
Eligibility criteria
- 1Used Zantac or generic ranitidine — Did you regularly take Zantac or generic ranitidine for at least 30 days between 2000-2020?
- 2U.S. consumer — Did you purchase or receive the medication in the United States?
Documents you'll need
- Pharmacy purchase record OR prescription record (if available)
- Sworn declaration of regular use
- Government-issued photo ID