Suppliers / Atabay Kimya Sanayi Ve Ticaret

Atabay Kimya Sanayi Ve Ticaret

Turkey Updated 9 July 2026

Atabay Kimya Sanayi Ve Ticaret is an API manufacturer based in Turkey. It holds one active US drug master file and one valid CEP across a filed portfolio of 2 molecules. Its GMP standing is certified by EMA.

1
active US DMFs
1
valid CEPs
4
registered plants
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Istanbul, Turkey Not on file
Gebze, Turkey Not on file
Kadikoy, Turkey Not on file
Gebze, Turkey Not on file

What they file, and where

Molecule Regulators Docs
Acetaminophen SFDA (Saudi Arabia), US FDA 2
Paracetamol EDQM 1

Also appears on these molecule pages

Acetaminophen API Paracetamol API

Filings and GMP by regulator

Regulator Filings GMP certificates
INVIMA (CO) 1 None
EMA None 5

Questions about Atabay Kimya Sanayi Ve Ticaret

Does Atabay Kimya Sanayi Ve Ticaret hold a US DMF or a CEP?
Atabay Kimya Sanayi Ve Ticaret holds 1 active US drug master file and 1 valid CEP. 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 Atabay Kimya Sanayi Ve Ticaret manufacture?
4 registered sites are on record, in Turkey (Istanbul, Gebze and Kadikoy among others). Every site is listed on this page with the register it came from.
What does Atabay Kimya Sanayi Ve Ticaret make?
2 molecules are on record against Atabay Kimya Sanayi Ve Ticaret, including Acetaminophen and Paracetamol. Each links through to that molecule's full manufacturer list.
Which regulators recognise Atabay Kimya Sanayi Ve Ticaret's GMP?
Current GMP certificates are on record from EMA. 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