Suppliers / Dragenopharm Apotheker Pueschl

Dragenopharm Apotheker Pueschl

Germany 56 employees Updated 9 July 2026

Dragenopharm Apotheker Pueschl is a finished-dose manufacturer based in Germany. It appears in 12 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), NAFDAC (NG) and NCELS (KZ). Its GMP standing is certified by ZLG (DE) and EMA.

0
active US DMFs
0
valid CEPs
3
registered plants
12
filings across 5 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
Tittmoning, United Arab Emirates Not on file
Tittmoning, United Arab Emirates Not on file
Tittmoning, Germany Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 6 None
NAFDAC (NG) 3 None
NCELS (KZ) 1 None
MINSA (CR) 1 None
EDE (AE) 1 None
ZLG (DE) None 4
EMA None 1

Questions about Dragenopharm Apotheker Pueschl

Does Dragenopharm Apotheker Pueschl hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dragenopharm Apotheker Pueschl. It does have 12 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dragenopharm Apotheker Pueschl manufacture?
3 registered sites are on record, in United Arab Emirates and Germany (Tittmoning among others). Every site is listed on this page with the register it came from.
Which regulators recognise Dragenopharm Apotheker Pueschl'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