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USFDA completes GMP inspection at Dr. Reddy's manufacturing facility in Hyderabad

17 Aug 2026 Evaluate

United States Food & Drug Administration (USFDA) has completed a GMP inspection at Dr. Reddy's Laboratories’ formulations manufacturing facility (FTO-3) in Bachupally, Hyderabad. The inspection was conducted from August 6, 2026 to August 14, 2026. The company has been issued a Form 483 with four observations, which we 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.


Peers
Company Name CMP
Sun Pharma. Inds. 1743.00
Dr. Reddys Labs. 1224.50
Cipla 1337.00
Lupin 1925.00
Zydus Lifesciences 1127.85
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