Suppliers / Zhejiang Yongtai Technology

Zhejiang Yongtai Technology

China 46 employees Updated 9 July 2026

Zhejiang Yongtai Technology is an API manufacturer based in China. It holds one active US drug master file.

1
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
China, China 3014271585

What they file, and where

Molecule Regulators Docs
Aspartic Acid US FDA 1

Also appears on these molecule pages

Questions about Zhejiang Yongtai Technology

Does Zhejiang Yongtai Technology hold a US DMF or a CEP?
Zhejiang Yongtai Technology holds 1 active US drug master file. 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.
Is Zhejiang Yongtai Technology FDA-registered?
One site operated by Zhejiang Yongtai Technology carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Zhejiang Yongtai Technology manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does Zhejiang Yongtai Technology make?
1 molecule is on record against Zhejiang Yongtai Technology, including Aspartic Acid. Each links through to that molecule's full manufacturer list.

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.

Comparing suppliers?

Choose your molecules and target markets. Zhejiang Yongtai Technology comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability