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Aurobindo Pharma Facility Gets Revised FDA Warning Letter

Aurobindo Pharma logoAurobindo Pharma
Sig2.68Sen-3.23Env0.00Soc0.00Gov-4.25

Aurobindo Pharma said its Telangana-based formulation manufacturing Unit-I, operated by wholly owned subsidiary Eugia Pharma Specialities, received a revised warning letter from the US FDA. The FDA inspection from Jan 27 to Feb 6, 2026 resulted in 11 observations for the injectable-drugs facility. The company said existing US supplies are not impacted, and Unit-I contributes 2% of group revenue.

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