www.fdanews.com/articles/163139-merck-gets-fda-nod-for-intravenous-noxafil
Merck Gets FDA Nod for Intravenous Noxafil
March 17, 2014
The FDA has approved Merck’s Noxafil 18 mg/mL antifungal injection for use against invasive Aspergillus and Candida infections in high-risk patients ages 18 and older, the drug giant said.
Friday’s approval for an intravenous version of Noxafil (posaconazole) adds to Merck’s already available 100 mg delayed-release tablets and 40 mg/mL oral suspension, both of which are indicated for patients ages 13 and older.
Merck plans to make the intravenous drug commercially available in the U.S. in mid-April. — Lena Freund
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