December 22, 2006 - The US Food and Drug Administration (FDA) has approved safety label revisions to advise of the expected similarity of levetiracetam's safety profile in patients with juvenile ...
Nov. 10, 2004 — The U.S. Food and Drug Administration (FDA) approved in August revisions to drug safety labeling to advise healthcare professionals of the following changes: estradiol transdermal ...
Naropin 2% Launched in New Freeflex Containers Fresenius Kabi announced that the Food and Drug Administration (FDA) has approved the launch of Naropin (ropivacaine HCl) injection in the company's ...
Södertälje, Sweden, 3 March 2004 - AstraZeneca announced today that its long-acting local anaesthetic Naropin® (ropivacaine) 5.0 mg/ml was recommended for approval in all EU member states for a new ...