Suppliers / Dr. Pfleger Arzneimittel

Dr. Pfleger Arzneimittel

Germany 192 employees Updated 9 July 2026

Dr. Pfleger Arzneimittel is an API and finished-dose manufacturer based in Germany. It holds one valid CEP. Its filings concentrate with EMA, MPA (SE) and ARCSA (EC). Its GMP standing is certified by ZLG (DE), ANVISA (Brazil) and EMA.

0
active US DMFs
1
valid CEPs
1
registered plants
44
filings across 8 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
BAMBERG, Germany Not on file

What they file, and where

Molecule Regulators Docs
Trospium Chloride EDQM 1

Also appears on these molecule pages

Adapalene finished dose Methenamine finished dose Methionine finished dose Terazosin finished dose Trospium API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 33 1
MPA (SE) 2 None
ARCSA (EC) 2 None
INVIMA (CO) 2 None
UZPHARM (UZ) 2 None
DMP (NO) 1 None
ZLG (DE) None 6
ANVISA (Brazil) None 1

Questions about Dr. Pfleger Arzneimittel

Does Dr. Pfleger Arzneimittel hold a US DMF or a CEP?
Dr. Pfleger Arzneimittel holds 1 valid CEP. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Dr. Pfleger Arzneimittel manufacture?
1 registered site is on record, in Germany (Bamberg). Every site is listed on this page with the register it came from.
What does Dr. Pfleger Arzneimittel make?
1 molecule is on record against Dr. Pfleger Arzneimittel, including Trospium Chloride. Each links through to that molecule's full manufacturer list.
Which regulators recognise Dr. Pfleger Arzneimittel's GMP?
Current GMP certificates are on record from ZLG (DE), 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