Cetirizine hydrochloride NEW

nCapacity: This project is one of our mature industrialized API projects, which is stable in high quality and capacity. Currently, the production capacity is around 6 tons/year. 

nQuality System: Registration of Drug Master File (DMF) with the U.S. FDA is undergoing. Meanwhile, our quality system is enhanced to qualify the on-site audit by the U.S. FDA. 

nPotential Partners: The prestigious pharmaceutical company Johnson & Johnson has conducted on-site audits twice at our facilities and is expected to become a partner in the future. 

nSeeking Collaborations: Formulation-related regulatory submissions and sales agency for API.