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Sun Pharma and Lupin receive FDA approvals for generic Cymbalta

December 12, 2013 | Natasha Alperowicz

Sun Pharmaceutical Industries (Mumbai) and Lupin (Mumbai), two leading pharma producers for the global markets, announced today that their US subsidiaries have gained FDA approvals for duloxetine hydrochloride delayed release drug, the generic version of the antidepressant  Cymbalta.  Cymbalta delayed-release capsule 20, 30 and 60 mg is an Eli Lilly product with last year’s sales in the United States approaching $5.5 billion.   Sun Pharma in the year ended 31 March 2013 reported sales of $2.1 billion of which $1.1 billion were in the US...

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