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Aurobindo receives tentative approval for zidovudine tablet
Aurobindo’s products included in World Health Organization (WHO) Pre-qualification list
Aurobindo’s scientist conferred award
Aurobindo posts revenue of Rs.2807 Million in Q1.
Aurobindo gets EDQM approval for Domperidone & Domperidone Maleate
Canadian authority approves Aurobindo’s facilities
Aurobindo Pharma gets US FDA nod for lamivudine and zidovudine combination tablets
Aurobindo receives - first generic approval of Efavirenz
Aurobindo announces approval of Stavudine tablets
Aurobindo records revenue of Rs.11592 Million. Record facility approvals, DMFs/ANDAs filings and significant R & D expenses weigh on Aurobindo's bottom line
Aurobindo receives second ANDA approval from US FDA for PEPFAR
Aurobindo receives the first ARV approval from US FDA
USFDA approval received for Unit VIII Facility
Aurobindo receives NABL approval for its Clinical Laboratory
Aurobindo in Forbes list
Best under a Billion - Asia's Rising Companies
Aurobindo receives US FDA approval for Citalopram
A robust generic product portfolio to unveil.
Aurobindo obtains two product approvals from US FDA
Records Rs.272 crore turnover in Q2
First product approval from US FDA received
Foray into Regulated Market crosses first major milestone
Company scientists conferred awards
Speech by the Chairman, Mr. P. V. Ramaprasad Reddy at the Annual General Meeting on 31st July 2004
Aurobindo posts Rs.2873 Millions sales and Rs.180 Million profit
Aurobindo net profit at Rs. 127 crs surges by 23%
UK MHRA (UK MCA) approval received for Unit 3
Subscription to preferential issue of equity shares
Aurobindo Q3 PAT grows by 68% Exports soar to 51% of sales
Aurobindo gets its first CoS approval from EDQM & files DMF for Citalopram
Aurobindo's Q2 Net Profit jumps to Rs.321.5 million, spurt by 57%
Preferential Issue of Equity Shares
Aurobindo net profit spurts by 52.75% in Q1
Aurobindo crosses the landmark Net Profit of Rs.100 crores
Aurobindo's demonstration of R&D leadership in cephalosporins
Aurobindo Pharma launches cefepime
Second quarter profit jumps  41.13%
Aurobindo implementing ERP package
First quarter profit jumps 34%
Aurobindo posts Net Profit of  Rs. 68.51 crores
Noted Cardiologist Dr. I. Satyamurthy joins Aurobindo Board
Aurobindo Pharma wins award for the best bulk drug company
Shares allotted to Templeton
Brazilian GMP certification received for the speciality generic formulations unit
Aurobindo Pharma acquires equity in Ranit Pharma
Mr. Lanka Srinivas inducted as Additional Director on Board of Aurobindo Pharma
Aurobindo Pharma launches Aztreonam for the first time in India  
Aurobindo Pharma & Citadel promote a joint venture  
Aurobindo Pharma welcomes excise duty exemption on anti-HIV drugs in budget
Aurobindo launches Cefactam (Cefoperazone plus Salbactam)
4th generation Cephalosporin – Cefpirome launched
Impressive Q3 performance 
Aurobindo shareholders approve Rs.125 crore Private Placement
Templeton to pick up equity
Aurobindo Pharma Board approves Rs. 125 crore private placement
Aurobindo Pharma launches two more antiretroviral products for HIV treatment
Restructuring on track
Aurobindo introduces two more drugs for treatment of Aids
Imunus Aurobindo launches two new anti-aids drugs
Aurobindo Pharma slashes prices of anti-aids drugs
Restructuring of Facilities
Income crosses Rs. 1000 crore land mark

www.aurobindo.com

Hyderabad, 15th January, 2005

AUROBINDO RECORDS IMPROVED PERFORMANCE QUARTER ON QUARTER
SUCCESSFUL USFDA INSPECTION OF ONE MORE UNIT
OBTAINS 3rd PRODUCT APPROVAL FROM USFDA

 

The total income for the third quarter ended 31st December 2004 stood at Rs. 323.34 crore (Rs.325.39 crore) and the net profit after taxation stood at Rs.10.59 crore (Rs.35.62 crore). During Q2 FY04-05, the total income and net profit after taxation were Rs.271.98 crore and Rs.2.56 crore respectively. When compared with Q2 FY04-05 results, the total income in Q3 FY 04-05 was up by 18.88 % and net profit after tax was up by 313.68%.
During the quarter, higher interest of Rs.10.42 crore (Rs.7.81 crore) and depreciation of Rs.12.58 crore (Rs.9.09 crore) were absorbed. These higher expenses were on account of investments in R&D and production infrastructure for regulatory markets.
The Company has also written off R&D expenditure of Rs.10.37 crore (Rs.8.14 crore) during the quarter.
The Company has accelerated the DMF/ANDA filings programme and the Q3 FY04-05 witnessed 11 DMFs filings (cumulative 64) and 5 ANDA/Formulation dossier filings (cumulative 15) in the US/EU. In US itself, the Company has filed 7 DMFs (cumulative 22) and 5 ANDAs (cumulative 11) in Q3.
During the quarter, another major milestone has been crossed in its foray into the regulated markets with the successful inspection and audit of the manufacturing facility - Unit 8 by USFDA without receiving any Form 483 queries. The Unit 8 located near Hyderabad, manufactures Active Pharmaceutical Ingredients (API) and comprises 3 manufacturing blocks. The company has filed 6 Drug Master Files (DMFs) from this unit in the therapeutic segments of CVS, CNS and Anti Retrovirals.
Aurobindo receives USFDA approval for Metformin:
Aurobindo Pharma Limited is pleased to announce that USFDA (U.S. Food and Drug Administration) has granted approval for its Abbreviated New Drug Application (ANDA) for Metformin. Metformin is indicated in the treatment of diabetes.
Both API and Formulation shall be manufactured in the Company’s Units and Aurobindo has distinctive advantage of complete vertical integration in this product in India. With this approval, Aurobindo Pharma has received its 3rd product approval from USFDA for marketing in the USA and looks forward for more to come in the near future.
The product is one among the top products in terms of volume in USA.
Aurobindo has invested significant resources in building a mega infrastructure for API’s and Formulations to emerge as a vertically integrated pharmaceutical company. Aurobindo’s 4 units for API’s and 4 Units for Formulations, are designed for the Regulated market. The Company expects to reap the benefits of continuous product approvals from US/EU in the coming quarters.

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