Suppliers / Acino Pharma

Acino Pharma

Switzerland Updated 9 July 2026

Acino Pharma is a finished-dose manufacturer based in Switzerland. It appears in 199 regulatory filings across 15 regulators, without an active US DMF or CEP on file. Its filings concentrate with NMRC (NA), SFDA (Saudi Arabia) and RAMA (GE). Its GMP standing is certified by EMA and NAFDAC (NG). Customs aggregates show $531K of exports covering 6 molecules to 1 destination in 2022.

0
active US DMFs
0
valid CEPs
4
registered plants
199
filings across 15 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
Liesberg, United Arab Emirates Not on file
Aesch Bl, Switzerland Not on file
Liesberg, Switzerland Not on file
Liesberg Switzerland, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NMRC (NA) 50 None
SFDA (Saudi Arabia) 39 None
RAMA (GE) 31 None
MINSA (CR) 18 None
ARCSA (EC) 16 None
EMA 10 2
NAFDAC (NG) None 2

Scale

Year Revenue Exports Destinations
2022 Not reported $531K 1

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 We do not publish the identity of any buyer.

Questions about Acino Pharma

Does Acino Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Acino Pharma. It does have 199 filings with 15 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Acino Pharma manufacture?
4 registered sites are on record, in United Arab Emirates, Switzerland and Nigeria (Liesberg, Aesch Bl and Liesberg Switzerland among others). Every site is listed on this page with the register it came from.
Which regulators recognise Acino Pharma's GMP?
Current GMP certificates are on record from EMA and NAFDAC (NG). 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
Customs aggregates
Export values, molecule and destination counts