When compliance is critical, our cGMP, US-manufactured VYCERIN* API Glycerin, USP, is your solution.
When compliance is critical, our cGMP, US-manufactured VYCERIN* API Glycerin, USP, is your solution. Listed with the U.S. Food and Drug Administration (FDA) under Drug Master File (DMF #040171), VYCERIN API Glycerin, USP can be used when glycerin functions as an active ingredient in a formulation.
As the leading U.S. supplier with more than 30 years’ experience in manufacturing glycerin at our world-scale Chicago oleochemical facility, Vantage offers several high-quality ingredients for a wide range of formulations that accelerate our customers’ time to market and enable their success.
In addition to Glycerin, Vantage is a leading manufacturer of Polyethylene Glycols (PEG), including LUMULSE PEG 400 NF/FCC—a versatile polymer that complies with the updated 2025 USP monograph for EG and DEG testing. It features low impurity levels to support customer compliance with state regulations. LUMULSE PEG 400 NF/FCC is suitable for use as an excipient in a wide range of pharmaceutical products and medications, helping to enhance drug delivery systems.
Contact us today to discuss Vantage solutions for your pharmaceutical formulation needs.
