Suppliers / Sandoz Industrial Products

Sandoz Industrial Products

Spain Updated 9 July 2026

Sandoz Industrial Products is an API manufacturer based in Spain. It holds 6 active US drug master files across a filed portfolio of 5 molecules. Its GMP standing is certified by AEMPS (ES).

6
active US DMFs
0
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Barcelona, Spain Not on file

What they file, and where

Molecule Regulators Docs
Ampicillin US FDA 2
Piperacillin US FDA 2
Amoxicillin US FDA 1
Cloxacillin US FDA 1
Potassium Clavulanate SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Amoxicillin API Ampicillin API Cloxacillin API Piperacillin API Potassium Clavulanate API

Filings and GMP by regulator

Regulator Filings GMP certificates
AEMPS (ES) None 1

Questions about Sandoz Industrial Products

Does Sandoz Industrial Products hold a US DMF or a CEP?
Sandoz Industrial Products holds 6 active US drug master files. 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 Sandoz Industrial Products manufacture?
1 registered site is on record, in Spain (Barcelona). Every site is listed on this page with the register it came from.
What does Sandoz Industrial Products make?
5 molecules are on record against Sandoz Industrial Products, including Ampicillin, Piperacillin, Amoxicillin and Cloxacillin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Sandoz Industrial Products's GMP?
Current GMP certificates are on record from AEMPS (ES). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates