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AUROBINDO PHARMA LTD. - 524804 - Announcement under Regulation 30 (LODR)-Acquisition

Company has incorporated a new step-down subsidiary in Russia
26-07-2023

Aurobindo Pharma hits 52-week high on FDA clean chit to Telangana unit

The United States Food and Drug Administration (USFDA) inspected the Unit I, a Formulation manufacturing facility, of Eugia Pharma Specialities
26-07-2023
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AUROBINDO PHARMA LTD. - 524804 - Completion Of US FDA Inspection At Unit I Of Eugia Pharma Specialities Ltd

Completion of US FDA Inspection at Unit I of Eugia Pharma Specialities Limited with classification of No Action Indicated
26-07-2023

Aurobindo Pharma arm gets USFDA nod for Plerixafor injection

The approval granted by the US Food Drug Administration (USFDA) is to manufacture and market Plerixafor Injection of strengths 24 mg/1.2 mL (20 mg/mL), single-dose vial, Aurobindo Pharma said in a regulatory filing.
25-07-2023
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AUROBINDO PHARMA LTD. - 524804 - Announcement under Regulation 30 (LODR)-Press Release / Media Release

Press Release in connection with USFDA approval received by Eugia Pharma Specialities Limited, a wholly owned subsidiary of the Company.
25-07-2023

Aurobindo Pharma gets 3 observations from USFDA, stock rebounds from early losses

The observations are procedural in nature and we will respond to the USFDA within the stipulated timelines, company said in its release.
24-07-2023
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AUROBINDO PHARMA LTD. - 524804 - Completion Of US FDA Inspection At Our Unit III - Reg.,

Completion of US FDA Inspection at Company''s Unit III
21-07-2023
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USFDA indicates voluntary action for Aurobindo Pharma's AP Plant

The U.S. regulator conducted an inspection of unit XIVfrom May 15 to 19, 2023.
17-07-2023
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AUROBINDO PHARMA LTD. - 524804 - Classification Of US FDA Inspection At Our Unit XIV, Anakapalli District, Andhra Pradesh - Reg

The Company''s Unit XIV has received EIR classifying the facility as voluntary action indicated.
17-07-2023
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