Lupin receives US FDA approval for prucalopride tablets
The news for ANDA
Global pharma major Lupin Limited (Lupin) announced that it has received approval from the United States Food and Drug Administration (FDA) for its Abbreviated New Drug Application for prucalopride tablets, 1 mg, and 2 mg. Prucalopride tablets are bioequivalent to Motegrity tablets, 1 mg and 2 mg, of Takeda Pharmaceuticals USA. Inc. This product will be manufactured at Lupin’s Goa facility in India.
The company: Lupin Limited
• Lupin Limited is a global pharmaceutical leader headquartered in Mumbai, India, with products distributed in over 100 markets.
• Lupin specializes in pharmaceutical products, including branded and generic formulations, complex generics, biotechnology products, and active pharmaceutical ingredients.
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