Suppliers / Zhejiang East-Asia Pharmaceutical

Zhejiang East-Asia Pharmaceutical

China Updated 9 July 2026

Zhejiang East-Asia Pharmaceutical is an API manufacturer based in China. It holds 3 valid CEPs across a filed portfolio of 3 molecules. Its filings concentrate with MINSA (CR), NAFDAC (NG) and UZPHARM (UZ). Its GMP standing is certified by MFDS (Korea).

0
active US DMFs
3
valid CEPs
3
registered plants
11
filings across 3 regulators

Registered plants

Site FDA FEI
Taizhou, China Not on file
Pubagang, China Not on file
Taizhou, China Not on file

What they file, and where

Molecule Regulators Docs
Levofloxacin EDQM 1
Terbinafine EDQM 1
Trimebutine EDQM 1

Also appears on these molecule pages

Terbinafine API Trimebutine API Levofloxacin API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 7 None
NAFDAC (NG) 3 None
UZPHARM (UZ) 1 None
MFDS (Korea) None 4

Questions about Zhejiang East-Asia Pharmaceutical

Does Zhejiang East-Asia Pharmaceutical hold a US DMF or a CEP?
Zhejiang East-Asia Pharmaceutical holds 3 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Zhejiang East-Asia Pharmaceutical manufacture?
3 registered sites are on record, in China (Taizhou and Pubagang among others). Every site is listed on this page with the register it came from.
What does Zhejiang East-Asia Pharmaceutical make?
3 molecules are on record against Zhejiang East-Asia Pharmaceutical, including Levofloxacin, Terbinafine and Trimebutine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Zhejiang East-Asia Pharmaceutical's GMP?
Current GMP certificates are on record from MFDS (Korea). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates