August 25, 2020
August 25, 2020 – RLC Labs has issued a voluntary recall of all lots within expiry of Nature-Throid® (Thyroid
USP Tablets) and WP Thyroid® (Thyroid USP Tablets). The manufacturer has found that
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August 24, 2020
August 24, 2020 – The U.S. FDA has approved an expanded indication for Mirena® (levonorgestrel)
intrauterine device (IUD), manufactured by Bayer. The product is now indicated for use
August 20, 2020
August 20, 2020 – The U.S. FDA has approved Kesimpta® (ofatumumab), manufactured by Novartis, to treat adults who have relapsing forms of multiple sclerosis (MS), to include clinically
August 20, 2020
August 20, 2020 – Bayshore Pharmaceuticals has issued a voluntary recall of one lot of Metformin Hydrochloride Extended-Release (ER) Tablets USP, 500mg, as well as one lot of Metformin
August 20, 2020
August 20, 2020 – The U.S. FDA has approved expanded indications for Kyprolis® (carfilzomib – Amgen)
and Darzalex® (daratumumab – Genmab). The drugs may now be used together
August 20, 2020
August 20, 2020 – The U.S. FDA has approved label changes for products that contain hydrochlorothiazide (HCTZ). The changes advise patients and healthcare professionals of
August 19, 2020
August 19, 2020 – The U.S. FDA has approved Mylan’s generic version of Tecfidera® (dimethyl fumarate –
Biogen) delayed release 120mg and 240mg capsules. Dimethyl fumarate
August 19, 2020
August 19, 2020 – The U.S. FDA has approved an expanded indication for Xeomin® (incobotulinumtoxinA)
intramuscular or intraglandular injection, manufactured by Merz Pharmaceuticals.