how do i know if my losartan has been recalled wellbutrin sr

Editor's note: This story on the recall of certain blood pressure medications has been updated numerous times since it was first published on July 24, 2018. Date 06/2020.Torrent's recall was expanded on Jan. 22 to include 10 additional lots of losartan potassium tablets, and six lots of losartan potassium and hydrochlorothiazide tablets. The drugs were made in India and distributed by Heritage Pharmaceuticals of East Brunswick, NJ. Between November 2018 and April 2019, close to 300 lots of drugs containing losartan were recalled because potentially cancer-causing substances were found in …

A recall of common blood pressure medication losartan has been expanded for a fifth time after manufacturer Torrent Pharmaceuticals found a possibly carcinogenic impurity in more batches of the drug, federal health officials said.Three additional lots of losartan potassium tablets and two additional lots of losartan potassium/hydrochlorothiazide tablets were The lots contained levels of N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) above the acceptable daily intake levels determined by the FDA. Torrent further expanded the recall in April for 36 more lots of losartan potassium tablets and 68 lots of losartan potassium/hydrochlorothiazide tablets. In April, the agency  released a list of 40 blood pressure medications it says are free from contamination. Golden State re-packages the tablets under its own label for retail sale. Remember that not all losartan products were affected by this recall. The patent has expired, and various pharmaceutical companies now produce the drug. If your medication is part of this recall, do not stop taking your medication yet.

However, not all ARBs have been affected, and patients should continue to use their medication, the FDA says. An additional 3.6 million prescriptions were written for irbesartan that year. If you are taking the popular blood pressure drug, losartan, you may have seen the news reports about contamination. A recall of common blood pressure medication losartan has been expanded for a fifth time after manufacturer Torrent Pharmaceuticals found a possibly carcinogenic impurity in … What do I do if my medication was recalled? FDA scientists concluded there would be one more cancer case above average rates for every 8,000 people on the highest dose of valsartan for four years. Talk to your healthcare provider first to determine the next steps. The International Agency for Research on Cancer, reports NDEA is used to make liquid rocket fuel and is … Here’s what you need to know.In November, the FDA announced a voluntary recall of losartan potassium/hydrochlorothiazide, 100 mg/25 mg tablets in 1,000-count plastic bottles, NDC 0781-5207-10, Lot number JB8912, Exp. For details on the recalled drugs, In each case, a recalled drug was contaminated with N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine (NDEA) or N-Nitroso N-Methyl 4-amino butyric acid (NMBA).NDEA is used to make rocket fuel and can also be found in some food and drinking water, but at low levels. © 2020 USA TODAY, a division of Gannett Satellite Information Network, LLC. In September, Torrent announced that an additional three lots of losartan potassium tablets in 100 mg and 50 mg doses, and two lots of losartan potassium/hydrochlorothiazide tablets 50 mg/12.5 mg, and 100 mg/25 mg are being recalled as well. Macleods Pharmaceuticals Limited on Feb. 25 recalled one lot of losartan potassium/hydrochlorothiazide combination tablets 100mg/25mg, with a July 2019 expiration date. Not every manufacturer is affected, nor every batch from those that are.

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