Suppliers / Syngen Biotech

Syngen Biotech

Taiwan Updated 9 July 2026

Syngen Biotech is an API manufacturer based in Taiwan. It holds one active US drug master file.

1
active US DMFs
0
valid CEPs
0
registered plants
7
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Mupirocin SFDA (Saudi Arabia), US FDA 2

Also appears on these molecule pages

Mupirocin API

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 7 None

Questions about Syngen Biotech

Does Syngen Biotech hold a US DMF or a CEP?
Syngen Biotech 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.
What does Syngen Biotech make?
1 molecule is on record against Syngen Biotech, including Mupirocin. Each links through to that molecule's full manufacturer list.
Where does Syngen Biotech file?
Filings are on record with NPRA (MY), 7 in total.

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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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