Suppliers / Alcon Laboratories

Alcon Laboratories

United States 2 duplicate records merged Updated 9 July 2026

Alcon Laboratories is a finished-dose manufacturer based in United States. It appears in 226 regulatory filings across 22 regulators, without an active US DMF or CEP on file. Its filings concentrate with MEDSAFE (NZ), EDE (AE) and DIGEMAPS (DO).

0
active US DMFs
0
valid CEPs
5
registered plants
226
filings across 22 regulators

Registered plants

Site FDA FEI
Fort Worth, United Arab Emirates Not on file
Cork, United Arab Emirates Not on file
Georgia, United Arab Emirates Not on file
Jeddah, Saudi Arabia Not on file
Riyadh, Saudi Arabia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MEDSAFE (NZ) 52 None
EDE (AE) 39 None
DIGEMAPS (DO) 26 None
US FDA 23 None
SAHPRA (ZA) 21 None
NMRC (NA) 11 None

Questions about Alcon Laboratories

Does Alcon Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Alcon Laboratories. It does have 226 filings with 22 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Alcon Laboratories manufacture?
5 registered sites are on record, in United Arab Emirates and Saudi Arabia (Fort Worth, Cork and Georgia among others). Every site is listed on this page with the register it came from.
Where does Alcon Laboratories file?
Filings are on record with MEDSAFE (NZ), EDE (AE), DIGEMAPS (DO), US FDA and 18 other regulators, 226 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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Open risk flags

  • 59 active litigation matters are on record.

Comparable suppliers

Aaa Pharmaceuticals also in United States Aarkish Pharmaceuticals NJ also in United States Abbott Laboratories also in United States Abon Pharmaceuticals also in United States Access Business Group also in United States

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