Suppliers / Dr. Paul Lohmann GmbH & Co. KGaA

Dr. Paul Lohmann GmbH & Co. KGaA

Germany Updated 9 July 2026

Dr. Paul Lohmann GmbH & Co. KGaA is an API manufacturer based in Germany. It appears in 2 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
4
registered plants
2
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
Lower Saxony, Germany Not on file
Lueneburg, Germany Not on file
Emmerthal, Germany Not on file
Emmerthal, Germany Not on file

What they file, and where

Molecule Regulators Docs
Ferrous SFDA (Saudi Arabia) 2
Magnesium SFDA (Saudi Arabia) 1
Manganese SFDA (Saudi Arabia) 1
Naglcerophosphate H2O SFDA (Saudi Arabia) 1
Sodium Glycerophosphate SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Ferrous API

Filings and GMP by regulator

Regulator Filings GMP certificates
NCELS (KZ) 2 None
ZLG (DE) None 18
EMA None 1

Questions about Dr. Paul Lohmann GmbH & Co. KGaA

Does Dr. Paul Lohmann GmbH & Co. KGaA hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dr. Paul Lohmann GmbH & Co. KGaA. It does have 2 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dr. Paul Lohmann GmbH & Co. KGaA manufacture?
4 registered sites are on record, in Germany (Lower Saxony, Lueneburg and Emmerthal among others). Every site is listed on this page with the register it came from.
What does Dr. Paul Lohmann GmbH & Co. KGaA make?
5 molecules are on record against Dr. Paul Lohmann GmbH & Co. KGaA, including Ferrous, Magnesium, Manganese and Naglcerophosphate H2O. Each links through to that molecule's full manufacturer list.
Which regulators recognise Dr. Paul Lohmann GmbH & Co. KGaA'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