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www.aurobindo.com |
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Hyderabad, 3rd April, 2006 |
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AUROBINDO RECEIVES APPROVAL FOR
CEFUROXIME AXETIL TABLETS |
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Aurobindo Pharma
Limited is pleased to announce that it has
received approval for Cefuroxime Axetil Tablets
USP, 125 mg (base), 250 mg (base), 500 mg (base)
from US FDA. |
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With this Oral Cephalosporin
approval, Aurobindo’s product basket for the US
market has increased to 13 (Final approvals).
Apart from this, the Company has 10 Tentative
Approvals for the US market. |
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The size of generics business
of Cefuroxime Axetil 125/250/500 mg is around
USD 50 Mn. |
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Cefuroxime Axetil tablets are
indicated for the treatment of patients with
infections caused by susceptible strains of
designated organisms in the following diseases:
Pharyngitis and Tonsillitis, Lower Respiratory
Tract Infections, Urinary Tract Infections and
Skin Structure Infections. |
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Cefuroxime Axetil Tablets USP,
125 mg (base), 250 mg (base), 500 mg (base) is
the generic version of Glaxo Wellcome's Ceftin®. |
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About Aurobindo Pharma Limited: |
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Aurobindo Pharma Limited (www.aurobindo.com),
headquartered at Hyderabad, India, manufactures
generic pharmaceuticals and active
pharmaceutical ingredients. The company has
received approvals for several facilities from
leading regulatory agencies like US FDA, UK MHRA,
WHO, Health Canada, MCC South Africa. The
company’s robust product portfolio is spread
over 6 major therapeutic/product areas
encompassing (Antibiotics, Anti-Retrovirals,
CVS, CNS, Gastroenterologicals, and Anti-Allergics)
around 65 APIs in the non-antibiotics and 55
APIs in the antibiotic segment. The Company is
marketing these products globally, in over 100
countries. |
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