Suppliers / Steroid

Steroid

Italy 58 employees 2 duplicate records merged Updated 9 July 2026

Steroid is an API manufacturer based in Italy. It holds 10 active US drug master files and 3 valid CEPs across a filed portfolio of 14 molecules.

10
active US DMFs
3
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Cologno Monzese, Italy Not on file

What they file, and where

Molecule Regulators Docs
Prednisolone SFDA (Saudi Arabia) 2
Beclometasone Dipropionate EDQM 1
Clascoterone US FDA 1
Difluprednate US FDA 1
Estradiol Valerate US FDA 1
Etonogestrel US FDA 1
Fulvestrant US FDA 1
Hydroxyprogesterone Caproate US FDA 1
Norethisterone US FDA 1
Testosterone EDQM 1
Show all 14 molecules on file
Testosterone Cypionate US FDA 1
Testosterone Enantate EDQM 1
Testosterone Enanthate US FDA 1
Testosterone Undecanoate US FDA 1

Also appears on these molecule pages

Estradiol API Etonogestrel API Fulvestrant API Norethisterone API Prednisolone API Testosterone API Testosterone Cypionate API Testosterone Undecanoate API

Questions about Steroid

Does Steroid hold a US DMF or a CEP?
Steroid holds 10 active US drug master files and 3 valid CEPs. 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 Steroid manufacture?
1 registered site is on record, in Italy (Cologno Monzese). Every site is listed on this page with the register it came from.
What does Steroid make?
14 molecules are on record against Steroid, including Prednisolone, Beclometasone Dipropionate, Clascoterone and Difluprednate. 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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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