Annora's Generic Mexiletine Hydrochloride Receives Approval in the U.S.
Zenara's Generic Ketorolac Tromethamine Receives Approval in the U.S.
Clinigen Healthcare is recalling three batches of Mexiletine hydrochloride hard capsules, indicated for the treatment of documented arrhythmias, due to a potential risk of under- or overdose, which could have consequences for the safety of patients. The Class 1 Medicines Recall Notification was published by the UK’s Medicines and Healthcare products Regulatory Agency (MHRA).
Global pharma major, Lupin Limited (Lupin) announced that it has entered into a distribution agreement with Medis for Lupin’s orphan drug NaMuscla (mexiletine). Medis will commercialize NaMuscla for the symptomatic treatment of myotonia in adults with non-dystrophic myotonic (NDM) disorders in Central and Eastern European countries. NaMuscla is the first and only licensed product for this indication.
ATLANTA, Jan. 27, 2022 /PRNewswire/ -- Senores Pharmaceuticals, Inc. announced the launch of Mexiletine Hydrochloride Capsules USP, 150 mg, 200 mg and 250 mg, a therapeutic equivalent version of MEXITIL (Mexiletine Hydrochloride) with one of the top 5 generic pharmaceutical companies in the U.S. market.
Havix's Generic Mexiletine Hydrochloride Receives Approval in the US
Slough, UK, 8 December 2020: Lupin welcomes the Scottish Medicines Consortium’s (SMC) decision to approve the use of NaMuscla® (mexiletine) for the treatment of symptomatic myotonia in adult patients with non-dystrophic myotonic disorders (NDM) in Scotland.1
Crossmedika SA`s Generic Mexiletine Hydrochloride Receives Approval in US
Lannett Company, Inc. (NYSE: LCI) today announced that it has launched Mexiletine Hydrochloride Capsules 150 mg, 200 mg and 250 mg, a partnered product. Mexiletine Hydrochloride Capsules is the AB-rated generic equivalent to Mexitil® Capsules of Boehringer Ingelheim.