Suppliers / Galderma Laboratories, L.P

Galderma Laboratories, L.P

United States Updated 9 July 2026

Galderma Laboratories, L.P is a finished-dose manufacturer based in United States. It appears in 61 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA, SAHPRA (ZA) and NMRC (NA).

0
active US DMFs
0
valid CEPs
1
registered plants
61
filings across 8 regulators

Registered plants

Site FDA FEI
Alby-sur-Cheran, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 21 None
SAHPRA (ZA) 15 None
NMRC (NA) 11 None
TGA (Australia) 4 None
INHRR (VE) 3 None
ARCSA (EC) 3 None

Questions about Galderma Laboratories, L.P

Does Galderma Laboratories, L.P hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Galderma Laboratories, L.P. It does have 61 filings with 8 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Galderma Laboratories, L.P manufacture?
1 registered site is on record, in United Arab Emirates (Alby-sur-cheran). Every site is listed on this page with the register it came from.
Where does Galderma Laboratories, L.P file?
Filings are on record with US FDA, SAHPRA (ZA), NMRC (NA), TGA (Australia) and 4 other regulators, 61 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability