Lupin has received approval from the United States Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA), Pregabalin Capsules, 25 mg, 50 mg, 75 mg, 100 mg, 150 mg, 200 mg, 225 mg and 300 mg to market a generic equivalent of Lyrica Capsules, 25 mg, 50 mg, 75 mg, 100 mg, 150 mg, 200 mg, 225 mg and 300 mg of Upjohn US 2 LLC. The product will be manufactured at Lupin's facility in Aurangabad, India.
Lupin Diagnostics is a part of Lupin Healthcare, which is a 100% subsidiary of Lupin. Meanwhile, Lupin is an innovation-led transnational pharmaceutical company headquartered in Mumbai, India.
