USA TODAY 0:00 0:43 A recall of common blood pressure medication losartan has been expanded for a fifth time after manufacturer Torrent Pharmaceuticals found a possibly carcinogenic 3/1/2019: UPDATE - Aurobindo expands its voluntary recall of valsartan and amlodipine/valsartan 3/1/2019: PRESS RELEASE - FDA provides update on its ongoing
Initiates Voluntary Nationwide Recall of Two (2) Lots of Quinapril and Hydrochlorothiazide Tablets USP 20mg/12
is conducting a voluntary recall of 80 lots of Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and
The inspection of the plant in February came just weeks after Aurobindo recalled 80 lots of valsartan because of the detection of N-nitrosodiethylamine (NDEA)
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is conducting a voluntary recall of 1 lot of Ranitidine Tablets 150mg to the retail level and 37 lots of Ranitidine Capsules 150mg, Ranitidine Capsules 300mg and Camber, Avet, Teva, and Torrent were affected by the recall
The recall later expanded to other “sartan” products as impurities turned up in the irbesartan API produced by India’s Aurobindo and in losartan products made using an API from China’s On November 8th, 2018 the FDA announced that Sandoz is recalling a single lot of Losartan/Hydrochlorothiazide Tablets 100mg/25mg at the consumer level due to an impurity detected in the recalled products
Torrent Pharmaceuticals Limited has expanded its voluntary recall of Losartan potassium tablets USP to include 6 lots of Losartan
The identifying NDC #s associated with Camber’s product as are follows: Losartan 25 mg 31722-700-90, 31722-700-05, 31722-700-10; Losartan 50 mg 31722-701-30, 31722-701
Amneal Pharmaceuticals
5mg, 5mg, and 10mg Read more
The affected product was packaged in 100-tablet bottles, has the NDC of Losartan Potassium Tablets 25 mg – 90/Bottle
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by calling 1-905-795-9437, extension 2201, or by email at orders@mintpharmaceuticals
If you buy a can of tomatoes or infant formula, you will find a Lot Number and a Use By/Expiration Date
Nitrosamines have previously been found in drugs to A