Suppliers / Palla Pharma Norway

Palla Pharma Norway

Norway 37 employees Updated 9 July 2026

Palla Pharma Norway is an API manufacturer based in Norway. It holds 2 valid CEPs. Its GMP standing is certified by EMA.

0
active US DMFs
2
valid CEPs
3
registered plants
0
filings across 0 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
KRAGERØ, Norway Not on file
Kragerø, Norway Not on file
Krageroe, Norway Not on file

What they file, and where

Molecule Regulators Docs
Codeine EDQM 2

Also appears on these molecule pages

Codeine API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1

Scale

Year Revenue Exports Destinations
2024 $19.8M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Questions about Palla Pharma Norway

Does Palla Pharma Norway hold a US DMF or a CEP?
Palla Pharma Norway holds 2 valid CEPs. 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 Palla Pharma Norway manufacture?
3 registered sites are on record, in Norway (Kragerø, Kragerø and Krageroe). Every site is listed on this page with the register it came from.
What does Palla Pharma Norway make?
1 molecule is on record against Palla Pharma Norway, including Codeine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Palla Pharma Norway's GMP?
Current GMP certificates are on record from 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
Company filings
Revenue as reported