Ranitidine and NDMA have been associated together since the 1980s. While there is no NDMA contamination in Zantac, but it consists of both nitrite and dimethylamine, which, when combined, form the compound NDMA. Unacceptable NDMA Levels in Zantac During June 2019, the FDA was notified by online pharmacy Valisure that routine tests conducted in their …
It was April 1st, 2020, when FDA announced that all manufacturers must withdraw the over the counter and prescription drugs containing ranitidine from the market, with immediate effect. Valisure Pharmacy suspected that NDMA levels in Zantac rose to incredibly high levels when exposed to higher temperatures and was confirmed by the FDA that this occurred …
FDA Request Removal of All Randitine Products Including Zantac! Read More »
Zantac’s potential to cause the formation of compounds in its users is being investigated by the U.S. the Food and Drug Administration, to escalate the risks posed by ranitidine, fully. With growing cancer worries from the high NDMA level inn Zantac/ranitidine, the medicine has been called off from across the States, and in fact, from …
FDA investigating NDMA? Recent Issues and happenings! Read More »
