Also, SLPA has regulatory compliance in place with respect to its formulation and API facility. The drug has a market size of USD885m (IQVIA MAT Q2 2018) with six other generic approvals, of which two approvals came in the last six months. For FY18, US sales stood at ~INR1.4b (USD20m; 19% of total sales), which came in largely from only two products (Capecitabine and Azacitidine). Thus, on FY18 base business of USD19m, g- Gleevec would contribute meaningfully in the US generic segment. Currently, SLPA has four ANDA approvals (including g-Gleevec) and a healthy pipeline of 34 products pending for approval. We expect US sales to reach INR3.2b in FY20 (32% of sales) on the back of new launches and better traction in approved molecules. facility located at Raichur received EIR for inspection, which was carried out in Jan18. The formulations facility at Jadcherla received EIR in Mar18 for inspection carried out in Dec17.