Suppliers / Zentiva Ks

Zentiva Ks

Czech Republic Updated 9 July 2026

Zentiva Ks is an API manufacturer based in Czech Republic. It holds 2 active US drug master files across a filed portfolio of 2 molecules.

2
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Articaine US FDA 1
Glyburide US FDA 1

Also appears on these molecule pages

Articaine API Glibenclamide API Glyburide API

Questions about Zentiva Ks

Does Zentiva Ks hold a US DMF or a CEP?
Zentiva Ks holds 2 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 Zentiva Ks make?
2 molecules are on record against Zentiva Ks, including Articaine and Glyburide. 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.

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Comparable suppliers

Apitoria Pharma shares 2 molecules Cambrex Profarmaco Milano shares 2 molecules Dipharma Francis shares 2 molecules Cadila Pharmaceuticals shares 2 molecules USV shares 2 molecules

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