Corporate News 03-Jul-23
Zydus' unit at Pharmex, Ahmedabad receives EIR from USFDA
Zydus Lifesciences has received the Establishment Inspection Report (EIR) from the USFDA for the inspection conducted at its manufacturing facility located at Pharmez, Ahmedabad from March 20 to 24, 2023. The inspection has been classified as Voluntary Action Indicated (VAI). The EIR report indicates that the inspection is closed.
Previous News
Sentynl, a Zydus company, acquires Zokinvy® (Lonafarnib)
( Corporate News - 04-May-24 10:42 )
Zydus Lifesciences receives USFDA approval for Dapsone Gel 7.5%
( Corporate News - 09-May-24 12:36 )
Zydus Life gets tentative USFDA nod for hypertension drugs
( Hot Pursuit - 14-Jun-24 12:34 )
Zydus receives USFDA tentative approval for Azilsartan Medoxomil and Chlorthalidone Tablets
( Corporate News - 14-Jun-24 13:42 )
Zydus Lifesciences Ltd soars 1.23%, gains for fifth straight session
( Hot Pursuit - 21-May-24 13:00 )
Zydus Lifesciences receives USFDA approval for Isosorbide Mononitrate ER Tablets
( Corporate News - 16-Feb-24 14:31 )
Zydus Life hits record high on USFDA nod for chest pain prevention drug
( Hot Pursuit - 16-Feb-24 16:53 )
Zydus receives USFDA tentative approval for Letermovir tablets
( Corporate News - 23-Mar-24 14:00 )
Zydus Lifesciences consolidated net profit rises 26.76% in the December 2023 quarter
( Results - Announcements 09-Feb-24 14:29 )
Zydus Lifesciences receives USFDA approval for Tadalafil Tablets
( Corporate News - 07-Jun-23 15:45 )
Zydus receives USFDA tentative approval for Edaravone Injection
( Corporate News - 14-Mar-24 13:51 )
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