The US Food and Drug Administration (US FDA) has completed a current good manufacturing practice (CGMP) inspection at ...
The US FDA had inspected Aurobindo's Unit-7 between January 28 and February 10, 2026. The inspection observations pointed to ...
The U.S. Food and Drug Administration (U.S. FDA) has issued nine observations to the oral solid dosage manufacturing unit of generic drugmaker Aurobindo Pharma near Hyderabad.
Aurobindo Pharma Limited recently informed that the United States Food and Drug Administration (USFDA) has completed an inspection at its Unit-VII manufacturing facility located ...
US FDA completes inspection of Anuh Pharma’s facilities at Tarapur MIDC with no Form 483 observations: Our Bureau, Bengaluru Monday, February 9, 2026, 15:30 Hrs [IST] US drug re ...
Eugia remains under FDA scrutiny as the unit of Indian drugmaker Aurobindo has received its fifth Form 483 since December. The company’s latest slap from the U.S. regulator stems from an April 25 to ...