Suppliers / Delpharm Lille S.A.S

Delpharm Lille S.A.S

France 169 employees Updated 9 July 2026

Delpharm Lille S.A.S is a finished-dose manufacturer based in France. It appears in 18 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), INVIMA (CO) and MINSA (CR). Its GMP standing is certified by ANSM (FR), ANVISA (Brazil) and EMA.

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
18
filings across 7 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Lys-Lez-Lannoy, France Not on file
LYS-LEZ-LANNOY, France Not on file
France, France 3007684549
Lys Lez Lannoy Cedex, France Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 5 None
INVIMA (CO) 4 None
MINSA (CR) 3 None
EDA (EG) 2 None
ARCSA (EC) 2 None
BOMRA (BW) 1 None
ANSM (FR) None 5
ANVISA (Brazil) None 3
EMA None 1

Scale

Year Revenue Exports Destinations
2024 $36.5M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Questions about Delpharm Lille S.A.S

Does Delpharm Lille S.A.S hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Delpharm Lille S.A.S. It does have 18 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Delpharm Lille S.A.S FDA-registered?
One site operated by Delpharm Lille S.A.S carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Delpharm Lille S.A.S manufacture?
4 registered sites are on record, in France (Lys-lez-lannoy, Lys-lez-lannoy and France among others). Every site is listed on this page with the register it came from.
Which regulators recognise Delpharm Lille S.A.S's GMP?
Current GMP certificates are on record from ANSM (FR), ANVISA (Brazil) and EMA. 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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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