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Progressive Pharma Push: Lupin Secures FDA Approval For Complex Generic
Lupin Limited has received U.S. FDA approval for its Glycerol Phenylbutyrate Oral Liquid, bioequivalent to Horizon’s Ravicti®. The therapy addresses urea cycle disorders (UCDs), a rare metabolic condition. With Ravicti® sales at USD 337 million in 2025, Lupin’s entry strengthens its U.S. generics portfolio.
Stay Ahead – Explore Now! World’s Fourth Largest Gold Miner’s IPO Paused Amid Market Concerns






