IGI Laboratories unveils US FDA approved nonsteroidal anti-inflammatory drug Diclofenac Sodium 1.5%.
M2 EQUITYBITES-July 10, 2015-IGI Laboratories unveils US FDA approved nonsteroidal anti-inflammatory drug Diclofenac Sodium 1.5%
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Pharmaceutical company IGI Laboratories (NYSE MKT:IG) revealed on Thursday the availability of its diclofenac sodium 1.5% topical solution in the US market.
This market launch follows the final approval from the US Food and Drug Administration (FDA) for an abbreviated new drug application (ANDA). The ANDA to the US FDA was originally filed in December 2010.
According to the company, it now markets seven products in 12 presentations in an IGI label.
The company added that the Diclofenac sodium topical solution 1.5% is a nonsteroidal anti-inflammatory drug indicated for the treatment of the pain from osteoarthritis of the knee.
Based on IMS Health data for May 2015, the total addressable market for this product is approximately USD13.3m, concluded the company.
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|Publication:||M2 EquityBites (EQB)|
|Date:||Jul 10, 2015|
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