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Thursday, September 25, 2008

Aurobindo Pharma receives final approval from USFDA

Aurobindo Pharma has received final approval from USFDA to manufacture and market Didanosine Delayed Release (enteric-coated) capsules 125mg, 200mg, 250mg and 400mg.

Didanosine Delayed Release capsules is the generic version of Bristol Myer Squibb's Videx EC (Didanosine) Delayed-release capsules, 125mg, 200mg, 250mg and 400mg and is indicated for the treatment of HIV-1 infections in adults. This is Aurobindo's 78th ANDA approval from the USFDA.

The company made this announcement during the trading hours today, 25 September 2008.

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