Suppliers / Siegfried Pharma

Siegfried Pharma

Switzerland Updated 9 July 2026

The public registers hold a second record for Siegfried Pharma. The fuller profile, with 94 active US DMFs and 40 valid CEPs, is at Siegfried. Figures on this page cover only this record.

Siegfried Pharma is an API manufacturer based in Switzerland. Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
ZOFINGEN, Switzerland Not on file

What they file, and where

Molecule Regulators Docs
Caffeine SFDA (Saudi Arabia) 1
Ephedrine SFDA (Saudi Arabia) 1
Tretinoin SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Caffeine API Ephedrine API Tretinoin API

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) None 1

Questions about Siegfried Pharma

Where does Siegfried Pharma manufacture?
1 registered site is on record, in Switzerland (Zofingen). Every site is listed on this page with the register it came from.
What does Siegfried Pharma make?
3 molecules are on record against Siegfried Pharma, including Caffeine, Ephedrine and Tretinoin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Siegfried Pharma's GMP?
Current GMP certificates are on record from ANVISA (Brazil). 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.

Comparing suppliers?

Choose your molecules and target markets. Siegfried Pharma comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Acino Pharma also in Switzerland Alpex Pharma also in Switzerland Baccinex also in Switzerland Bracco Suisse also in Switzerland Drossapharm also in Switzerland

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates