The strategy of the Hyderabad-based pharma major Dr Reddy's Laboratories' (DRL) to approach the US market with a series of gambles rather than on one major upside is paying dividends.

Drug maker, Aurobindo Pharma (Q,N,C,F)* has received the tentative approval for Donepezil Hydrochloride Tablets 5 mg and 10 mg (ANDA 90-056) from the US Food & Drug Administration (USFDA).

Sun Pharmaceutical Industries Ltd. on Monday announced that the US Food & Drug Administration (FDA) has granted its subsidiary an approval for its Abbreviated New Drug Application (ANDA) to market Roxicodone, oxycodone hydrochloride tablets.

Sun Pharmaceutical Industries Ltd. (524715.BY) has received U.S. Food & Drug Administration approval to make and sell generic versions of anticonvulsant topiramate tablets.