Lupin is recalling 1.11 lakh units of Duloxetine delayed-release capsules from the US market. The company is recalling 1,11,648 units of Duloxetine delayed-release capsules USP, in the strength of 30 mg, on account of failed dissolution specification. The drug was manufactured by Lupin in Goa plant. The ongoing voluntary nationwide recall is a class III recall.
Lupin is an innovation led transnational pharmaceutical company developing and delivering a wide range of branded & generic formulations, biotechnology products and APIs globally.