Suppliers / Baxter SA-NV

Baxter SA-NV

Belgium 5 duplicate records merged Updated 9 July 2026

Baxter SA-NV is a finished-dose manufacturer based in Belgium. It appears in 664 regulatory filings across 20 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, FAMHP (BE) and ANSM (FR). Its GMP standing is certified by EMA and SFDA (Saudi Arabia). Customs aggregates show $195K of exports covering 5 molecules to 2 destinations in 2025.

0
active US DMFs
0
valid CEPs
7
registered plants
664
filings across 20 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Dammam, United Arab Emirates Not on file
Lessines, Belgium Not on file
Opfikon, Switzerland Not on file
Riyadh, Saudi Arabia Not on file
Jeddah, Saudi Arabia Not on file
Riyadh, Saudi Arabia Not on file

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 300 None
FAMHP (BE) 151 None
ANSM (FR) 48 None
SWISSMEDIC (CH) 48 None
SFDA (Saudi Arabia) 35 1
INHRR (VE) 24 None
EMA None 3

Scale

Year Revenue Exports Destinations
2025 Not reported $195K 2
2024 Not reported $341K 2
2023 Not reported $647K 4
2022 Not reported $644K 2

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 We do not publish the identity of any buyer.

Questions about Baxter SA-NV

Does Baxter SA-NV hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Baxter SA-NV. It does have 664 filings with 20 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Baxter SA-NV manufacture?
7 registered sites are on record, in United Arab Emirates, Belgium, Switzerland and Saudi Arabia (Dammam, Lessines and Opfikon among others). Every site is listed on this page with the register it came from.
Which regulators recognise Baxter SA-NV's GMP?
Current GMP certificates are on record from EMA and SFDA (Saudi Arabia). 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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Comparable suppliers

Benechim also in Belgium Besins Manufacturing Belgium also in Belgium Catalent Belgium also in Belgium Cenexi - Laboratoires Thissen S. A also in Belgium Eumedica Pharmaceuticals also in Belgium

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
Customs aggregates
Export values, molecule and destination counts