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

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

Comparing suppliers?

Choose your molecules and target markets. Extrovis EU comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

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