US peptide API CDMO with facilities in the US and China.
- Model
- CDMO
- Manufacturer?
- Yes
Glucagon is a 29-amino-acid hormone used for severe hypoglycaemia.
3 listed companies hold an active US Type II Drug Master File for Glucagon API, based in United States (1), Switzerland (1), Italy (1). 2 have 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.
US peptide API CDMO with facilities in the US and China.
Swiss peptide and oligonucleotide CDMO with GMP plants in Europe and the US.
Fresenius Kabi's Italian API unit; its Villadose site near Venice develops and makes peptide APIs, also offered through Fresenius Kabi contract manufacturing. Holds US DMFs for 6 peptide APIs.
Companies holding active US DMFs for Glucagon include AmbioPharm, Bachem Holding AG and Fresenius Kabi iPSUM S.r.l.. Other manufacturers may supply it without a US DMF.
Among listed DMF holders: United States (1), Switzerland (1), Italy (1).
No. FDA reviews a DMF when a drug application references it and does not approve DMFs on their own.