Dr. Reddys Laboratories Ltd.

United States Food & Drug Administration (USFDA) has completed a GMP inspection at Dr. Reddy’s Laboratories’ API manufacturing facility (CTO-5) in Miryalaguda, Telangana, India. The inspection was conducted from May 19, 2025 to May 24, 2025. The company has been issued a Form 483 with 2 observations, which it will address within the stipulated timeline.

Dr. Reddy's Laboratories is a multinational pharmaceutical company based in Hyderabad, Telangana in India. It manufactures and markets a wide range of pharmaceuticals in India and overseas.