Lupin Receives U.S. FDA Approval for Glycerol Phenylbutyrate Oral Liquid
Glycerol Phenylbutyrate Oral Liquid, 1.1 grams per mL, is bioequivalent to the reference listed drug (RLD), Ravicti® Oral Liquid, 1.1 grams per mL, of Horizon Therapeutics U.S. Holding LLC. It is indicated for chronic management of patients with urea cycle disorders (UCDs) that cannot be managed by dietary protein restriction and/or amino acid supplementation alone.
The product sales for Glycerol Phenylbutyrate Oral Liquid (RLD Ravicti®) were
About Lupin
Lupin Limited is a global pharmaceutical leader headquartered in
To know more, visit www.lupin.com or follow us on LinkedIn https://www.linkedin.com/company/lupin
Ravicti® is the registered trademark of Horizon Therapeutics U.S. Holding LLC, a subsidiary of Amgen Inc.
View original content to download multimedia:https://www.prnewswire.com/news-releases/lupin-receives-us-fda-approval-for-glycerol-phenylbutyrate-oral-liquid-302762977.html
SOURCE Lupin Pharmaceuticals, Inc.
Serious News for Serious Traders! Try StreetInsider.com Premium Free!
You May Also Be Interested In
- Hedg3 Integrates Benzinga's Analyst Ratings Data Into Trading Platform
- Innovative Food Holdings, Inc. Announces Second Quarter 2026 Earnings Call
- Seabridge Gold Reports Gitxsan Government Has Called for Meaningful Consultation and Collaboration with Tsetsaut Skii km La Hax
Create E-mail Alert Related Categories
PRNewswire, Press ReleasesRelated Entities
FDASign up for StreetInsider Free!
Receive full access to all new and archived articles, unlimited portfolio tracking, e-mail alerts, custom newswires and RSS feeds - and more!



Tweet
Share