Suppliers / Ulkar Kimya Sanayii Ve Ticaret

Ulkar Kimya Sanayii Ve Ticaret

Turkey Updated 9 July 2026

Ulkar Kimya Sanayii Ve Ticaret is an API manufacturer based in Turkey. It holds 8 active US drug master files across a filed portfolio of 8 molecules.

8
active US DMFs
0
valid CEPs
0
registered plants
18
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Aripiprazole US FDA 1
Candesartan US FDA 1
Candesartan Cilexetil US FDA 1
Etodolac US FDA 1
Irbesartan US FDA 1
Lansoprazole US FDA 1
Olmesartan US FDA 1
Pantoprazole US FDA 1

Also appears on these molecule pages

Candesartan API Candesartan Cilexetil API Etodolac API Pantoprazole API Irbesartan API Lansoprazole API Olmesartan API Aripiprazole API

Filings and GMP by regulator

Regulator Filings GMP certificates
TITCK (TR) 18 None

Questions about Ulkar Kimya Sanayii Ve Ticaret

Does Ulkar Kimya Sanayii Ve Ticaret hold a US DMF or a CEP?
Ulkar Kimya Sanayii Ve Ticaret holds 8 active US drug master files. 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 Ulkar Kimya Sanayii Ve Ticaret make?
8 molecules are on record against Ulkar Kimya Sanayii Ve Ticaret, including Aripiprazole, Candesartan, Candesartan Cilexetil and Etodolac. Each links through to that molecule's full manufacturer list.
Where does Ulkar Kimya Sanayii Ve Ticaret file?
Filings are on record with TITCK (TR), 18 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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Comparable suppliers

Alembic Pharmaceuticals shares 2 molecules Zydus Lifesciences shares 2 molecules Zhejiang Huahai Pharmaceutical shares 2 molecules Zhuhai Rundu Pharmaceutical shares 2 molecules Matrix Pharmacorp shares 1 molecule

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