Suppliers / Lilly

Lilly

Spain LLY Updated 9 July 2026

Lilly is an API and finished-dose manufacturer based in Spain. It appears in 280 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA, AEMPS (ES) and MINSA (CR). Its GMP standing is certified by MFDS (Korea), ANVISA (Brazil) and US FDA, among 6 authorities. Its most recent recorded inspection, by US FDA, closed on 14 February 2024 as NAI.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
280
filings across 7 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 14 February 2024 NAI US FDA
  • 9 March 2021 VAI US FDA
  • 15 March 2018 VAI US FDA
  • 18 October 2013 NAI US FDA

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

Registered plants

Site FDA FEI
Alcobendas, United Arab Emirates Not on file
MADRID, Spain Not on file
Madrid, Spain Not on file
Madrid, Spain Not on file
Spain, Spain 3000235541

What they file, and where

Molecule Regulators Docs
Olanzapine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 191 1
AEMPS (ES) 71 1
MINSA (CR) 6 None
SFDA (Saudi Arabia) 5 None
NAFDAC (NG) 3 1
ANPP (DZ) 3 None
MFDS (Korea) None 2
ANVISA (Brazil) None 1
EMA None 1

Scale

Year Revenue Exports Destinations
2025 $65.2B Not reported Not reported
2024 $45.0B Not reported Not reported
2023 $34.1B Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer.

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Open risk flags

  • 20 active litigation matters are on record.
  • The most recent inspection outcome was NAI, on 14 February 2024.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Company filings
Revenue as reported