Corporate News 23-Feb-24
Suven Pharmaceuticals' Unit 3 & 5 clear USFDA inspection
Suven Pharmaceuticals announced that its Active Pharmaceutical Ingredients (API) and Formulations facilities (Unit-3 and Unit-5, respectively) in Pashamylaram, Hyderabad, India, have completed the Pre Approval Inspections (PAI) and Good Manufacturing Practices (GMP) inspections by the US Food & Drug Administration (US FDA) today. The inspection was conducted from 12 February 2024, to 23 February 2024, and no Form 483 has been issued as a result of the inspection
Previous News
Suven Pharmaceuticals to conduct board meeting
( Corporate News - 31-Jan-24 12:06 )
Suven Pharmaceuticals schedules board meeting
( Corporate News - 20-May-24 17:36 )
Suven Pharmaceuticals consolidated net profit rises 10.29% in the March 2022 quarter
( Results - Announcements 09-May-22 14:13 )
Suven Pharmaceuticals fixes record date for dividend
( Market Beat - Reports 09-May-22 20:14 )
Board of Suven Pharmaceuticals recommends special dividend
( Corporate News - 03-Sep-22 11:01 )
Suven Pharmaceuticals to convene AGM
( Corporate News - 10-May-22 15:08 )
Suven Pharmaceuticals announces board meeting date
( Corporate News - 30-Oct-21 11:45 )
Suven Pharmaceuticals fixes record date for final dividend
( Market Beat - Reports 09-Jun-21 10:46 )
Shares of Suven Pharmaceuticals gets listed
( Corporate News - 09-Mar-20 11:23 )
Suven Pharma to manufacture anti-covid drugs Molnupiravir and 2-DG
( Corporate News - 10-Jun-21 17:27 )
Suven Pharmaceuticals to conduct AGM
( Corporate News - 15-Jul-24 17:27 )
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