Home » FDA Approves Intravenous Formulation of AstraZeneca's Nexium
FDA Approves Intravenous Formulation of AstraZeneca's Nexium
The FDA has approved a new intravenous administration formulation of AstraZeneca's prescription proton pump inhibitor Nexium IV (esomeprazole magnesium).
The drug is now approved as an intravenous infusion or injection for the short-term treatment of gastroesophageal reflux disease patients, with a history of erosive esophagitis, who are unable to take capsules.
Nexium IV for injection is administered once daily as either a 10 to 30 minute intravenous infusion or by intravenous injection (no less than three minutes). Treatment is given for up to 10 days and does not require an in-line filter.
KEYWORDS Drug Pipeline Alert
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