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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 most of the targeted API and
formulation facilities from leading regulatory
agencies such as 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.
The formulation portfolio is built on six
technology platforms such as immediate release
generics, SR/CR generics, orally
disintegrating/mouth dissolving generics,
combination products, sterile/lyophilized
generics and liquids/dry syrups.
Aurobindo has filed over 100 DMFs
and 75 ANDAs for the USA market alone in
addition to filings in other countries. The pace
of filings is matched by rapid product approvals
from various markets. Till date Aurobindo has
received 38 ANDA approvals (both final and
tentative) from US FDA.
Aurobindo operates in over 100
countries and markets over 180 APIs and 250
formulations |