Suppliers / Bausch & Lomb

Bausch & Lomb

United States 4 duplicate records merged Updated 9 July 2026

Bausch & Lomb is a finished-dose manufacturer based in United States. It appears in 139 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, US FDA and EDE (AE). Its GMP standing is certified by US FDA, MHRA (UK) and ANVISA (Brazil). Its most recent recorded inspection, by US FDA, closed on 30 July 2025 as NAI.

0
active US DMFs
0
valid CEPs
7
registered plants 3 with an FDA FEI number
139
filings across 9 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
3 of 3 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 30 July 2025 NAI US FDA
  • 27 February 2025 OAI US FDA
  • 25 August 2023 NAI US FDA
  • 25 November 2019 VAI US FDA
  • 30 January 2019 NAI US FDA
  • 10 August 2018 OAI US FDA
  • 15 September 2017 NAI US FDA
  • 26 May 2017 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Clearwater, United Arab Emirates Not on file
Tampa, United Arab Emirates Not on file
Rochester, United Arab Emirates Not on file
TAMPA, United States Not on file
Greenville, United States 1032500
Rochester, United States 1317628

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 55 None
US FDA 36 2
EDE (AE) 16 None
DMP (NO) 13 None
NMPA (CN) 7 None
SFDA (Saudi Arabia) 5 None
MHRA (UK) None 2
ANVISA (Brazil) None 1

Questions about Bausch & Lomb

Does Bausch & Lomb hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Bausch & Lomb. It does have 139 filings with 9 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Bausch & Lomb FDA-registered?
3 sites operated by Bausch & Lomb carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Bausch & Lomb's last inspection go?
The most recent inspection on record closed on 30 July 2025 as NAI (No Action Indicated: nothing objectionable was found). 8 inspections are on file, of which 2 closed as OAI.
Where does Bausch & Lomb manufacture?
7 registered sites are on record, in United Arab Emirates and United States (Clearwater, Tampa and Rochester among others). Every site is listed on this page with the register it came from.
Which regulators recognise Bausch & Lomb's GMP?
Current GMP certificates are on record from US FDA, MHRA (UK) and ANVISA (Brazil). 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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Open risk flags

  • The most recent inspection outcome was NAI, on 30 July 2025.

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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