Dr Reddy’s gets fresh FDA notice as biologics scrutiny persists
India’s Dr Reddy’s Laboratories (NYSE: RDY) has received a fresh Form 483 from the US Food and Drug Administration, keeping regulatory scrutiny fixed on one of its biologics manufacturing sites just as the company pushes deeper into higher-value generics.
The FDA issued the notice after completing a pre-license inspection at Dr Reddy’s biologics manufacturing facility in Bachupally, Hyderabad.
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