Suppliers / MSD International

MSD International

Switzerland 3 duplicate records merged Updated 9 July 2026

MSD INTERNATIONAL is an API and finished-dose manufacturer based in Switzerland. It appears in 50 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), INHRR (VE) and MINSA (CR). Its GMP standing is certified by FDA (GH).

0
active US DMFs
0
valid CEPs
0
registered plants
50
filings across 4 regulators

What they file, and where

Molecule Regulators Docs
Doravirine SFDA (Saudi Arabia) 1
Mometasone Furoate SFDA (Saudi Arabia) 1
Posaconazole SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Indacaterol finished dose Letermovir finished dose Mometasone API Posaconazole API

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 22 None
INHRR (VE) 18 None
MINSA (CR) 9 None
INVIMA (CO) 1 None
FDA (GH) None 1

Questions about MSD International

Does MSD International hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for MSD International. It does have 50 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
What does MSD International make?
3 molecules are on record against MSD International, including Doravirine, Mometasone Furoate and Posaconazole. Each links through to that molecule's full manufacturer list.
Which regulators recognise MSD International's GMP?
Current GMP certificates are on record from FDA (GH). 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates