Suppliers / Unither Liquid Manufacturing

Unither Liquid Manufacturing

France Updated 9 July 2026

Unither Liquid Manufacturing is a finished-dose manufacturer based in France. It appears in 13 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), NAFDAC (NG) and ARCSA (EC). Its GMP standing is certified by ANSM (FR), EAEU_EEC and ANVISA (Brazil), among 5 authorities.

0
active US DMFs
0
valid CEPs
1
registered plants
13
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
COLOMIERS, France Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 4 None
NAFDAC (NG) 2 1
ARCSA (EC) 2 None
NPRA (MY) 2 None
MINSA (CR) 2 None
UZPHARM (UZ) 1 None
ANSM (FR) None 5
EAEU_EEC None 1
ANVISA (Brazil) None 1
EMA None 1

Scale

Year Revenue Exports Destinations
2024 $86.2M 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 We do not publish the identity of any buyer.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 Unither Liquid Manufacturing

Does Unither Liquid Manufacturing hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Unither Liquid Manufacturing. It does have 13 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Unither Liquid Manufacturing manufacture?
1 registered site is on record, in France (Colomiers). Every site is listed on this page with the register it came from.
Which regulators recognise Unither Liquid Manufacturing's GMP?
Current GMP certificates are on record from ANSM (FR), EEC (Eurasian Economic Union), ANVISA (Brazil), NAFDAC (NG) 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