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Flamel Technologies Announces FDA Approval of Bloxiverz

Posted 5 Jun 2013 by Drugs.com

LYON, FRANCE – (Marketwire) – 06/03/2013 – Flamel Technologies today announced that the U.S. Food and Drug Administration (FDA) has approved the company's New Drug Application (NDA) for Bloxiverz (neostigmine methylsulfate), a drug used intravenously in the operating room for the reversal of the effects of non-depolarizing neuromuscular blocking agents after surgery. Flamel expects to launch Bloxiverz in July 2013 in 0.5 and 1.0 mg/mL strengths. "We are extremely excited and pleased to receive this FDA approval for Bloxiverz, the first product from the portfolio of Éclat products acquired in March 2012," said Mike Anderson, Chief Executive Officer of Flamel. Bloxiverz is the first FDA-approved version of neostigmine, even though other versions of neostigmine have been on the market as unapproved, grandfathered products under the Food, Drug and Cosmetic Act of 1938. Today, ... Read more

Related support groups: Neostigmine, Reversal of Nondepolarizing Muscle Relaxants

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Related Condition Support Groups

Reversal of Neuromuscular Blockade, Myasthenia Gravis, Reversal of Nondepolarizing Muscle Relaxants, Urinary Retention

Related Drug Support Groups

Bloxiverz, Prostigmin, Prostigmin Bromide

Neostigmine Patient Information at Drugs.com