Company History
Your current location：首頁 > About Lonzeal > Company History2006 Lonzeal Pharmaceuticals was established
2008 The production base of Lonzeal Pharmaceuticals was put into operation
2010 Obtained the GMP certificate of raw materials from the State Food and Drug Administration of China
2012 Passed the GMP on-site inspection of the World Health Organization
From 2012 to 2015, API products have been registered in Brazil, Russia, South Africa and other countries
2017 Passed the GMP on-site inspection of multiple anti-AIDS APIs by the World Health Organization
2018 Zero defect passed the US FDA's API GMP on-site inspection
2019 Anti-AIDS and hepatitis B preparation products took the lead in passing the consistency evaluation
2021 Paroxetine Hydrochloride, Tenofovir Alafenamide Fumarate, and Pregabalin passed the consistency evaluation and obtained drug registration approval
Domestic sales center：17703115689 [email protected]
International Sales department：18034564568 [email protected]
Human Resource Center：0311-87512081 [email protected]
Address: Shenze County Industrial Park, Shijiazhuang City, Hebei Province (No. 16 West Ring Road)
