Suppliers / Extrovis EU

Extrovis EU

Switzerland 222 employees Updated 9 July 2026

Extrovis EU is an API manufacturer based in Switzerland. It holds 8 active US drug master files and one valid CEP across a filed portfolio of 8 molecules. Its filings concentrate with US FDA, EMA and FAMHP (BE).

8
active US DMFs
1
valid CEPs
1
registered plants
44
filings across 8 regulators

Registered plants

Site FDA FEI
Baar, Switzerland Not on file

What they file, and where

Molecule Regulators Docs
Dapsone EDQM, US FDA 2
Avibactam US FDA 1
Calcium Gluconate US FDA 1
Dipotassium Phosphate US FDA 1
Eltrombopag US FDA 1
Monopotassium Phosphate US FDA 1
Tolvaptan US FDA 1
Trabectedin US FDA 1

Also appears on these molecule pages

Avibactam API Dapsone API Eltrombopag API Tolvaptan API Trabectedin API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 24 None
EMA 5 None
FAMHP (BE) 4 None
AIFA (IT) 4 None
INFARMED (PT) 3 None
MPA (SE) 2 None

Questions about Extrovis EU

Does Extrovis EU hold a US DMF or a CEP?
Extrovis EU holds 8 active US drug master files 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 Extrovis EU manufacture?
1 registered site is on record, in Switzerland (Baar). Every site is listed on this page with the register it came from.
What does Extrovis EU make?
8 molecules are on record against Extrovis EU, including Dapsone, Avibactam, Calcium Gluconate and Dipotassium Phosphate. Each links through to that molecule's full manufacturer list.
Where does Extrovis EU file?
Filings are on record with US FDA, EMA, FAMHP (BE), AIFA (IT) and 4 other regulators, 44 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