Atorvastatin Calcium, Baloxavir Marboxil, Folic Acid

Company History

Specialized in producing cardiovasculaar pharmaceuticals and medicines, every year the output of APIs is more than 800 tons and finished formulations is more than 3000 million tablets.

IN1949
CPF is established in changzhou city in the year of 1949
IN1984
Our API, Hydrochlorothiazide was approved by U.S.FDA.
IN2006
Received CEP certificate for Hydrochlorothiazide
IN2013
Have approved by US. FDA audits for 9 times, passed EU GMP inspection 3 times
IN2014
Nantong Chanyoo passed EU GMP inspection
IN2015
Changzhou pharma. And Nantong Chanyoo approved by U.S. FDA, Changzhou wuxin approved by Chinese GMP.
IN2016
Rs tablets approved site inspection of U.S. FDA. Nantong Chanyoo approved by PMDA.
IN2017
Changzhou pharma. Approved by PMDA; finished formulation workshop approved by U.S. FDA.
IN2018
China GMP approved for both API and finished products again.
IN2019
Changzhou pharma and Nantong Chanyoo approved by FDA routine inspection.

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CPF is established in changzhou city in the year of 1949

Our API, Hydrochlorothiazide was approved by U.S.FDA.

Received CEP certificate for Hydrochlorothiazide

Have approved by US. FDA audits for 9 times, passed EU GMP inspection 3 times

Nantong Chanyoo passed EU GMP inspection

Changzhou pharma. And Nantong Chanyoo approved by U.S. FDA, Changzhou wuxin approved by Chinese GMP.

Rs tablets approved site inspection of U.S. FDA. Nantong Chanyoo approved by PMDA.

Changzhou pharma. Approved by PMDA; finished formulation workshop approved by U.S. FDA.

China GMP approved for both API and finished products again.

Changzhou pharma and Nantong Chanyoo approved by FDA routine inspection.

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