August 27, 2020
August 27, 2020 – The U.S. FDA has approved an expanded indication for Ultravate® (halobetasol
propionate) topical lotion, manufactured by Sun Pharmaceuticals. The product can now
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News
August 26, 2020
August 26, 2020 – The U.S. FDA has removed a black box warning for canagliflozin-containing products
regarding an increased risk of amputation. The warning was originally added to the drugs
August 25, 2020
August 25, 2020 – The U.S. FDA has approved Cystadrops® (cysteamine ophthalmic solution) 0.37%, manufactured by Recordati Rare Diseases, to treat corneal cystine crystal deposits in
August 25, 2020
August 25, 2020 – The U.S. FDA has approved Albuterol Sulfate Inhalation Aerosol 90mcg (base)/
actuation, manufactured by Lupin, as a generic for Teva’s ProAir® HFA. The product is
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
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