From the PharmaLive.com News Archive - Jun. 04, 2010
Mylan today announced that its subsidiary Matrix Laboratories Limited
has received final approval from the FDA for its ANDA for Gabapentin
Tablets USP, 600 mg and 800 mg, the generic version of Pfizer's
Neurontin Tablets for the treatment of postherpetic neuralgia, a
complication of shingles. The product will be distributed by Mylan
Pharmaceuticals. Gabapentin Tablets had U.S. sales of approximately
$174 million for the 12 months ending March 31, 2010.
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