Dr. Reddy's Receives FDA Tentative Approval for Zenavod Capsules, 40 mg for Treatment of Rosacea in Adults

Dr. Reddy's Laboratories

, announced today the U.S. Food and Drug Administration (US FDA) tentative approval for Zenavod™ (doxycycline) Capsules, 40 mg. Zenavod is a tetracycline-class drug indicated for the treatment of only inflammatory lesions (papules and pustules) of rosacea in adult patients. Promius™ Pharma, LLC, the U.S. subsidiary of India's Dr. Reddy's Laboratories will be responsible for commercializing Zenavod in the U.S. market. "This development confirms our ability and commitment to develop differentiated dermatology products leveraging the in-house capabilities of Promius Pharma, LLC and Dr. Reddy's," stated G V Prasad, CEO and Co-Chairman, Dr. Reddy's Laboratories. He continued, "We are pleased to receive a tentative FDA