Suppliers / Rousselot

Rousselot

Netherlands Updated 9 July 2026

Rousselot is an API manufacturer based in Netherlands. It holds one valid CEP.

0
active US DMFs
1
valid CEPs
2
registered plants
9
filings across 1 regulators

Registered plants

Site FDA FEI
Boulogne Billancourt, France Not on file
Son En Breugel, Netherlands Not on file

What they file, and where

Molecule Regulators Docs
Gelatin EDQM 1

Also appears on these molecule pages

Gelatin API

Filings and GMP by regulator

Regulator Filings GMP certificates
EEC_EAEU 9 None

Questions about Rousselot

Does Rousselot hold a US DMF or a CEP?
Rousselot holds 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 Rousselot manufacture?
2 registered sites are on record, in France and Netherlands (Boulogne Billancourt and Son En Breugel). Every site is listed on this page with the register it came from.
What does Rousselot make?
1 molecule is on record against Rousselot, including Gelatin. Each links through to that molecule's full manufacturer list.
Where does Rousselot file?
Filings are on record with EEC (Eurasian Economic Union), 9 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability