Suppliers / Peptido

Peptido

Germany 14 employees Updated 9 July 2026

Peptido is an API manufacturer based in Germany. It holds 2 active US drug master files and 2 valid CEPs across a filed portfolio of 2 molecules. Its GMP standing is certified by ZLG (DE).

2
active US DMFs
2
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Bexbach, Germany Not on file

What they file, and where

Molecule Regulators Docs
Levothyroxine EDQM, SFDA (Saudi Arabia), US FDA 3
Liothyronine Sodium EDQM, US FDA 2

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
ZLG (DE) None 4

Questions about Peptido

Does Peptido hold a US DMF or a CEP?
Peptido holds 2 active US drug master files and 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 Peptido manufacture?
1 registered site is on record, in Germany (Bexbach). Every site is listed on this page with the register it came from.
What does Peptido make?
2 molecules are on record against Peptido, including Levothyroxine and Liothyronine Sodium. Each links through to that molecule's full manufacturer list.
Which regulators recognise Peptido's GMP?
Current GMP certificates are on record from ZLG (DE). 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