Suppliers / Four 20 Pharma

Four 20 Pharma

Germany 36 employees Updated 9 July 2026

Four 20 Pharma is a finished-dose manufacturer based in Germany. It appears in 7 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by ZLG (DE) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
7
filings across 1 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
North Rhine-Westphalia, Germany Not on file
Paderborn, Germany Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDA (EG) 7 None
ZLG (DE) None 6
EMA None 1

Questions about Four 20 Pharma

Does Four 20 Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Four 20 Pharma. It does have 7 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Four 20 Pharma manufacture?
2 registered sites are on record, in Germany (North Rhine-westphalia and Paderborn). Every site is listed on this page with the register it came from.
Which regulators recognise Four 20 Pharma's GMP?
Current GMP certificates are on record from ZLG (DE) 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