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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 records improved performance quarter on quarter
Successful USFDA Inspection of one more Unit
Obtains 3rd product approval from USFDA
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 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, 31st July, 2004

AUROBINDO POSTS RS.2873 MILLIONS SALES AND RS.180 MILLION PROFIT RECEIVES US FDA APPROVAL FOR TWO OF ITS UNITS AND OBTAINS 2 MORE COS FROM EDQM

 
Aurobindo Pharma reported a total income of Rs.2872.9 Millions (Rs.3076.1 Millions) for the first quarter ended 30th June 2004.

The gross profit before interest, depreciation and exchange fluctuations has grown by 22.3% and stood at Rs.502.7 Millions (Rs.411.2 Millions).

The profit after interest, depreciation but before exchange fluctuations has grown by 14% and stood at Rs.319.3 Millions (Rs.280.5 Millions).
After accounting for exchange fluctuation of Rs.82.3 Millions, the net profit stood at Rs.180.2 Millions (Rs.230.5 Millions).
The comparative financial results are as under:
 

(Rs. in Millions)

  Q1 FY 04-05 Q1 FY 03-04
Gross profit before exchange rate fluctuations 502.7 411.2
Less: Interest 73.6 60.0
  Depreciation
109.8 70.7
Profit before exchange rate fluctuations 319.3 280.5
Exchange rate fluctuation (loss)/gain (82.3) 39.0
Provision for taxes 56.8 89.0
Profit after tax 180.2 230.5
The broad product mix strategy and accruing cost efficiencies enabled  the company to  post an impressive growth of  22% in gross profit before exchange fluctuations inspite of  the price pressures in Pen G related products which reduced the total turnover to Rs.2872.9 Millions (Rs.3076.1 Millions), increased R&D expenditure of Rs.87.8 Millions (Rs.43.4 Millions), and increased depreciation of Rs.109.8 Millions (Rs.70.7 Millions).

Developments in R&D and regulatory approvals:

Aurobindo has achieved the land mark in its efforts to enter regulated markets by receiving the US FDA approvals for Unit 1 (APIs) and Unit 3 (Formulations).
Aurobindo has been working on five major product platforms (SSPs, Cephalosporins, CVS, CNS, Antivirals) to develop a robust revenue model in regulated markets. More than 15 products are targeted in each product platform. Its facility/product approvals received in the area of Cephalosporins, CVS, CNS, Antivirals platforms are important milestones in its efforts to penetrate regulated markets. Four API sites (Unit1, Unit 6, Unit 8 and Unit 11) are going to be the back bone of API strategy. Five formulation sites (Unit 3A/ 3B, Unit 6 B, Unit 12, JV at Los Angeles) will drive the formulation strategy.
The Company has filed 5 DMFs and 2 ANDAs for the US markets. Similarly the Company has filed 22 EDMFs/COS for EU markets.
The R&D strength has increased to 391 to create the planned product portfolio. Eminent scientists in the area of IPR, Chemical & Formulation Research are driving the R&D.  Eight more patents are filed in the Q1 making the cumulative filings to 77. Ten more DMFs/COS are filed making the total filings to 41 in regulated markets. The cumulative ANDAs/Dossiers filed in US and EU increased to 6 (CNS -3 and CVS – 3). Aurobindo is developing a broad portfolio of ANDAs/DMFS in all five product platforms, both in sterile and non sterile products, using all the nine units.
Top management professionals with successful track record have joined Aurobindo operations in US and EU to accomplish the marketing success.
The growing scientific strength, robust product mix with five product platforms and one of the largest manufacturing infrastructure in APIs/Formulations will position Aurobindo in a unique position to exploit the potential in injectable and oral formulations opportunity in the world.

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