Suppliers / Sandoz

Sandoz

Switzerland Updated 9 July 2026

The public registers hold a second record for Sandoz. The fuller profile, with 40 active US DMFs and 20 valid CEPs, is at Sandoz. Figures on this page cover only this record.

Sandoz is a finished-dose manufacturer based in Switzerland. It appears in 6,466 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), EMA and MPA (SE). Customs aggregates show $188.6M of exports covering 2,928 molecules to 48 destinations in 2025.

0
active US DMFs
0
valid CEPs
0
registered plants
6,466
filings across 4 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
AIFA (IT) 6,142 None
EMA 311 None
MPA (SE) 9 None
INFARMED (PT) 4 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $16.5M 30
2025 Not reported $188.6M 48
2024 Not reported $159.7M 52
2023 Not reported $179.2M 54

Export figures are customs aggregates. We do not publish the identity of any buyer.

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Sandoz

Does Sandoz hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sandoz. It does have 6,466 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sandoz file?
Filings are on record with AIFA (IT), EMA, MPA (SE) and INFARMED (PT), 6,466 in total.

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.

Comparing suppliers?

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

Start for free
No sales call.

Comparable suppliers

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
Customs aggregates
Export values, molecule and destination counts