Is Steroid S.p.A. FDA approved?

Steroid S.p.A. holds 1 FDA-registered establishment in Italy. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Steroid S.p.A.'s drugs manufactured?

The FDA register lists Cologno Monzese. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, packaging.

What drugs does Steroid S.p.A. make?

13 products are listed under Steroid S.p.A. in the openFDA NDC Directory, most often as powder; injection, solution; injection. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Steroid S.p.A.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 13
Labeller names: 2
Live patents: 0
Countries: 1
Base: Italy

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Labelling1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Steroid S.p.A.	Viale Spagna 156, Cologno Monzese, 20093, Italy (ITA)	Analytical testing, Active ingredient (API) manufacture, Labelling, Packaging	3002808258428086292

Catalogue

Drug listings by form and route

13 active NDC listings: 13 bulk ingredient. By marketing category: BULK INGREDIENT 12, BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING 1.

Dosage form	NDCs
powder	8
injection, solution	2
injection	1
liquid	1
tablet	1

Route	NDCs

Labeller name on the listing	NDCs
steroid s.p.a.	11
steroid spa	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Boldenone Undecylenate	liquid	49803-009BULK INGREDIENT
-	Difluprednate	powder	49803-002BULK INGREDIENT
-	Estradiol Cypionate	powder	49803-007BULK INGREDIENT
-	Estradiol Valerate	powder	49803-013BULK INGREDIENT
-	Etonogestrel	tablet	49803-012BULK INGREDIENT
-	Fulvestrant	injection	49803-011BULK INGREDIENT
-	Hydoxyprogesterone Caproate	powder	49803-001BULK INGREDIENT
-	Oxymetholone	powder	49803-008BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-	Stanozolol	powder	49803-004BULK INGREDIENT
-	Testosterone Cypionate	injection, solution	49803-006BULK INGREDIENT
-	Testosterone Decanoate	powder	49803-010BULK INGREDIENT
-	Testosterone Enanthate	injection, solution	49803-005BULK INGREDIENT
-	Testosterone Undecanoate	powder	49803-003BULK INGREDIENT

Compare

Comparable companies in Italy

Industriale Chimica SRL1 site · 74 NDC
Farmabios S.p.A.1 site · 69 NDC
CAMBREX PROFARMACO MILANO SRL1 site · 43 NDC
PROCOS SpA1 site · 42 NDC
BSP Pharmaceuticals SpA1 site · 40 NDC
Chiesi USA, Inc.1 site · 25 NDC
Archimica S.p.A.1 site · 22 NDC
Chemo Biosynthesis s.r.l.1 site · 18 NDC
Societa Italiana Medicinali Scandicci S.I.M.S. SrL1 site · 12 NDC
Corden Pharma Bergamo SpA1 site · 10 NDC

Enquiry

Common questions

Is Steroid S.p.A. FDA approved?: Steroid S.p.A. holds 1 FDA-registered establishment in Italy. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Steroid S.p.A.'s drugs manufactured?: The FDA register lists Cologno Monzese. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, packaging.
What drugs does Steroid S.p.A. make?: 13 products are listed under Steroid S.p.A. in the openFDA NDC Directory, most often as powder; injection, solution; injection. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.