Aurobindo Pharma receives approval from South African Health Products Regulatory Authority for latest fixed dose triple combination tablets

Aurobindo Pharma Limited is pleased to announce that the company has received approval from the South African Health Products Regulatory Authority (SAHPRA) for its Dolutegravir, Lamivudine and Tenofovir Disoproxil Fumarate (DLT) tablets, 50mg/300mg/300mg, the first-line preferred regimen for HIV patients as per latest WHO guidelines. Aurobindo is now among the first few companies which has received approval for this product. This approval demonstrates our commitment towards HIV patients and enables the company to participate in South African HIV tender as well as launch in private market. The approval further strengthens Aurobindo’s HIV product basket in South Africa, which has the potential to improve the lives of millions of patients.