Suppliers / Yung Zip Chemical Ind

Yung Zip Chemical Ind

Taiwan 4102.TWO Updated 9 July 2026

Yung Zip Chemical Ind is an API manufacturer based in Taiwan. It holds 19 active US drug master files and 2 valid CEPs across a filed portfolio of 12 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 28 July 2023 as VAI.

19
active US DMFs
2
valid CEPs
2
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
Inspections
4 of 4 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 28 July 2023 VAI US FDA
  • 29 June 2018 VAI US FDA
  • 16 January 2015 VAI US FDA
  • 4 May 2012 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Taichung, Taiwan Not on file
Taiwan, Taiwan 3002808540

What they file, and where

Molecule Regulators Docs
Diclofenac EDQM, US FDA 6
Acyclovir US FDA 2
Mefenamic Acid EDQM, US FDA 2
Metoprolol US FDA 2
Miconazole US FDA 2
Clonidine US FDA 1
Clopidogrel US FDA 1
Deferasirox US FDA 1
Econazole US FDA 1
Edaravone US FDA 1
Show all 12 molecules on file
Rivaroxaban US FDA 1
Zolpidem US FDA 1

Also appears on these molecule pages

Acyclovir API Clonidine API Deferasirox API Diclofenac API Econazole API Edaravone API Mefenamic Acid API Metoprolol API Miconazole API Zolpidem API Clopidogrel API Rivaroxaban API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about Yung Zip Chemical Ind

Does Yung Zip Chemical Ind hold a US DMF or a CEP?
Yung Zip Chemical Ind holds 19 active US drug master files and 2 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.
Is Yung Zip Chemical Ind FDA-registered?
One site operated by Yung Zip Chemical Ind 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.
How did Yung Zip Chemical Ind's last inspection go?
The most recent inspection on record closed on 28 July 2023 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 4 inspections are on file.
Where does Yung Zip Chemical Ind manufacture?
2 registered sites are on record, in Taiwan (Taichung and Taiwan). Every site is listed on this page with the register it came from.
What does Yung Zip Chemical Ind make?
12 molecules are on record against Yung Zip Chemical Ind, including Diclofenac, Acyclovir, Mefenamic Acid and Metoprolol. Each links through to that molecule's full manufacturer list.
Which regulators recognise Yung Zip Chemical Ind's GMP?
Current GMP certificates are on record from US FDA. 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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Open risk flags

  • The most recent inspection outcome was VAI, on 28 July 2023.

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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