Meda AB: Sublinox Registration Application Submitted to the FDA

STOCKHOLM, Sweden--(BUSINESS WIRE)--Regulatory News: The registration application for Sublinox has been submitted to the US Food and Drug Administration (FDA). Sublinox (treatment of insomnia) contains zolpidem, a well-documented active substance, which is one of the world’s most used substances for this disorder. Sublinox uses a unique, patented sublingual tablet formulation for fast, effective absorption. A recent phase III study confirmed that Sublinox gave faster onset of action than other zolpidem tablet formulations.