Suppliers / Mylan S.A.S

Mylan S.A.S

France Updated 9 July 2026

Mylan S.A.S is a finished-dose manufacturer based in France. It appears in 114 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANSM (FR), ANPP (DZ) and MPA (SE).

0
active US DMFs
0
valid CEPs
0
registered plants
114
filings across 6 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
ANSM (FR) 44 None
ANPP (DZ) 23 None
MPA (SE) 20 None
INFARMED (PT) 16 None
EMA 9 None
DMP (NO) 2 None

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 Mylan S.A.S

Does Mylan S.A.S hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mylan S.A.S. It does have 114 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Mylan S.A.S file?
Filings are on record with ANSM (FR), ANPP (DZ), MPA (SE), INFARMED (PT) and 2 other regulators, 114 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.

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Comparable suppliers

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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