Is Archimica S.p.A. FDA approved?

Archimica 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 Archimica S.p.A.'s drugs manufactured?

The FDA register lists LODI. Registered operations: analytical testing, active ingredient (API) manufacture.

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

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

Archimica S.p.A.

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

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Registered sites: 1
Active NDC listings: 22
Live patents: 0
Countries: 1
Base: Italy

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Archimica S.p.A.	VIALE MILANO 86, LODI, - 26900, Italy (ITA)	Analytical testing, Active ingredient (API) manufacture	3002874947429351620

Catalogue

Drug listings by form and route

22 active NDC listings: 22 bulk ingredient. By marketing category: BULK INGREDIENT 22.

Dosage form	NDCs
powder	22

Route	NDCs

Labeller name on the listing	NDCs
archimica s.p.a.	22

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Bromfenac Sodium Salt Sesq Hydrate	powder	55512-0013BULK INGREDIENT
-	Capecitabine	powder	55512-0015BULK INGREDIENT
-	Cytarabine	powder	55512-0026BULK INGREDIENT
-	Disopyramide Phosphate	powder	55512-0004BULK INGREDIENT
-	Glycerylphosphorylcholine Anhydrous	powder	55512-0022BULK INGREDIENT
-	Hydralazine Hydrochloride	powder	55512-0010BULK INGREDIENT
-	Hydroxyurea	powder	55512-0003BULK INGREDIENT
-	Oxcarbazepine	powder	55512-0006BULK INGREDIENT
-	Oxcarbazepine	powder	55512-0007BULK INGREDIENT
-	Oxcarbazepine	powder	55512-0008BULK INGREDIENT
-	Oxcarbazepine	powder	55512-0016BULK INGREDIENT
-	Oxcarbazepine	powder	55512-0017BULK INGREDIENT
-	Oxcarbazepine	powder	55512-0018BULK INGREDIENT
-	Oxcarbazepine	powder	55512-0023BULK INGREDIENT
-	Pentetrazole	powder	55512-0024BULK INGREDIENT
-	Pirenzepina Base Pura	powder	55512-0025BULK INGREDIENT
-	Sucralfate	powder	55512-0002BULK INGREDIENT
-	Sucralfate	powder	55512-0009BULK INGREDIENT
-	Sucralfate	powder	55512-0019BULK INGREDIENT
-	Sucralfate	powder	55512-0020BULK INGREDIENT
-	Sucralfate	powder	55512-0021BULK INGREDIENT
-	Sulfapyridine	powder	55512-0001BULK INGREDIENT

Compare

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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
Chemo Biosynthesis s.r.l.1 site · 18 NDC
Steroid S.p.A.1 site · 13 NDC
Societa Italiana Medicinali Scandicci S.I.M.S. SrL1 site · 12 NDC
Corden Pharma Bergamo SpA1 site · 10 NDC

Enquiry

Common questions

Is Archimica S.p.A. FDA approved?: Archimica 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 Archimica S.p.A.'s drugs manufactured?: The FDA register lists LODI. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does Archimica S.p.A. make?: 22 products are listed under Archimica S.p.A. in the openFDA NDC Directory, most often as powder. 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.