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17 August 2026 at 9:18 am
Summary
Aurobindo Pharma's Raleigh manufacturing plant in the US has received a 'Voluntary Action Indicated' (VAI) classification from the US FDA, allowing applications for inhalers and other products to proceed. This classification follows the closure of the inspection of the facility.
Aurobindo Pharma's US Subsidiary Lannett Company LLC Faces Four USFDA Observations
24 Aug 2026, 1:27 pm · Pharmaceuticals
Aurobindo Pharma Arm Eugia Pharma's Telangana Unit Receives USFDA Warning Letter
14 Aug 2026, 4:08 pm · Healthcare
Aurobindo Pharma Q1 net profit jumps 25% to ₹1,032 crore, three arms to merge
5 Aug 2026, 9:59 pm · finance
Aurobindo Pharma Sets Up Manufacturing Subsidiary in Indonesia
11 Jul 2026, 1:24 am · business
Dr Reddy's Explores Biosimilars and Innovation for Future Growth
25 Aug 2026, 12:20 am · Pharmaceuticals
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