Swiss peptide and oligonucleotide CDMO with GMP plants in Europe and the US.
- Model
- CDMO
- Manufacturer?
- Yes
Triptorelin is a GnRH agonist (Trelstar, Decapeptyl).
3 listed companies hold an active US Type II Drug Master File for Triptorelin API, based in Switzerland (2), United States (1). 1 has a regulator record of GMP manufacturing.
Ordered by score. Scores follow the published rules and are not affected by paid placement. Updated 2026-11-13.
Source: FDA Drug Master File list. Holding a DMF is a regulatory filing, not an FDA approval.
Swiss peptide and oligonucleotide CDMO with GMP plants in Europe and the US.
California peptide synthesizer maker founded 1993 that also runs a cGMP peptide CDMO site in Milpitas; US DMF for triptorelin.
Swiss Debiopharm plant in Martigny making triptorelin sustained-release products; US DMF for triptorelin pamoate microgranules.
Companies holding active US DMFs for Triptorelin include Bachem Holding AG, C S Bio Co (CSBio) and Debiopharm Research & Manufacturing SA. Other manufacturers may supply it without a US DMF.
Among listed DMF holders: Switzerland (2), United States (1).
No. FDA reviews a DMF when a drug application references it and does not approve DMFs on their own.