Tuesday October 17th 2017

FDA gives final approval to Perrigo’s ANDA for repaglinide tablets 1 mg and 2 mg

Perrigo Company plc today announced that it has received final approval from the U.S. Food & Drug Administration for its abbreviated new drug application for repaglinide tablets 1 mg and 2 mg, the generic equivalent to Prandin Tablets (repaglinide tablets) and has commenced shipment of product. Perrigo previously launched the 0.5 mg strength in 2013.

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FDA gives final approval to Perrigo’s ANDA for repaglinide tablets 1 mg and 2 mg

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