Liraglutide API manufacturers

Liraglutide is a GLP-1 receptor agonist; the active ingredient of Victoza and Saxenda.

20 listed companies hold an active US Type II Drug Master File for Liraglutide API, based in China (8), India (7), Switzerland (2), United States (1), Taiwan (1), Italy (1). 14 have a regulator record of GMP manufacturing, and 1 carries an open FDA warning letter.

Ordered by score. Scores follow the published rules and are not affected by paid placement. Updated 2026-11-13.

Liraglutide API DMF holders (20)

Source: FDA Drug Master File list. Holding a DMF is a regulatory filing, not an FDA approval.

GMP

Tianjin unit of Asymchem, a CDMO listed in Shenzhen and Hong Kong that makes peptides and oligos; US DMFs for liraglutide and semaglutide.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedCDMO
Auro Peptides Ltd
Sangareddy (near Hyderabad), India
High
GMP

Peptide API subsidiary of Aurobindo Pharma with a plant near Hyderabad. Makes generic peptide APIs and runs GMP contract projects from mg to kg scale.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping
Biocon Ltd
Bengaluru, India
High
GMP

Bengaluru biopharma company that makes generic APIs and complex formulations, including GLP-1 peptides. Holds US DMFs for liraglutide, semaglutide and tirzepatide.

Model
Manufacturer
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping
GMP

Indian CDMO whose Turbhe, Navi Mumbai site develops and makes peptide APIs by solid- and solution-phase synthesis. Holds US DMFs for 9 peptide APIs.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping
High
GMP

Raichur API and CDMO subsidiary of Shilpa Medicare; US DMFs for desmopressin, liraglutide and octreotide; Raichur units inspected by US FDA in 2025.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleCDMO
High
GMP

Jiangsu peptide CDMO and generic API supplier with large automated SPPS capacity; states it has passed four US FDA inspections. Holds US DMFs for 9 peptide APIs.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping
AmbioPharm
North Augusta, South Carolina, USA
High
GMPCOA

US peptide API CDMO with facilities in the US and China.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionInternational Shipping
Bachem Holding AG
Bubendorf, Switzerland
High
GMPCOA

Swiss peptide and oligonucleotide CDMO with GMP plants in Europe and the US.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionInternational Shipping
Hybio Pharmaceutical
Shenzhen, China
High
GMP

Chinese peptide drug manufacturer producing APIs and finished products.

Model
Manufacturer
Manufacturer?
Yes
GMP CertifiedIn-House Production
PolyPeptide Group
Baar, Switzerland (sites in SE, BE, FR, US, IN)
High
GMPCOA

Peptide-focused CDMO running GMP manufacturing sites on three continents.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionInternational Shipping
ScinoPharm Taiwan
Tainan, Taiwan
High
GMP

API manufacturer and CDMO focused on complex generics, including peptides.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House Production
High

Beijing API company, founded 2006, that holds DMFs and has its APIs made in partner facilities under its own quality control. Holds US DMFs for 13 peptide APIs.

Model
Manufacturer
Manufacturer?
Yes
WholesaleInternational Shipping

Chongqing maker of diabetes and obesity drugs, active since 2015 and controlled by Zhifei (300122) since 2025; US DMFs for liraglutide and semaglutide.

Model
Manufacturer
Manufacturer?
Yes
In-House ProductionWholesale
Fresenius Kabi iPSUM S.r.l.
Villadose (Rovigo), Italy
High

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.

Model
CDMO
Manufacturer?
Yes
In-House ProductionWholesaleInternational Shipping

Hangzhou recombinant drug maker listed in Hong Kong (02566), formerly Huadong Medicine's gene engineering centre; US DMF for liraglutide.

Model
Manufacturer
Manufacturer?
Yes
In-House ProductionWholesale
GMP

Mumbai peptide API maker acquired by Piramal Pharma in 2021; its oxytocin API is WHO-prequalified; US DMF for oxytocin.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleCDMO
GMP

Shenzhen peptide CDMO and API maker founded in 2009, with 13 cGMP lines and 85,000 L of SPPS/LPPS reactor volume. Holds US DMFs for 6 peptide APIs.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping

Suzhou peptide API and formulation maker founded in 2000, flagship of Tianma Pharma Group, offering CRO/CMO/CDMO services. Holds US DMFs for 8 peptide APIs.

Model
CDMO
Manufacturer?
Yes
In-House ProductionWholesaleInternational Shipping
Medium

Navi Mumbai biopharma and specialty pharma company; US DMFs for lanreotide and liraglutide.

Model
Manufacturer
Manufacturer?
Yes
In-House ProductionWholesale
GMP

Mumbai-based generics group that makes APIs and finished medicines. Holds US Type II DMFs for 15 peptide APIs, including GLP-1s and GnRH analogues.

Notice: open regulatory issue
Model
Manufacturer
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping

Other peptide APIs

Related

Frequently asked questions

Who manufactures Liraglutide API?

Companies holding active US DMFs for Liraglutide include Asymchem Life Science (Tianjin) Co., Ltd, Auro Peptides Ltd, Biocon Ltd, Piramal Pharma Ltd (Piramal Pharma Solutions), Shilpa Pharma Lifesciences Ltd, Sinopep-Allsino Biopharmaceutical Co., Ltd., AmbioPharm, Bachem Holding AG, Hybio Pharmaceutical, PolyPeptide Group and 10 more. Other manufacturers may supply it without a US DMF.

Where are Liraglutide API manufacturers based?

Among listed DMF holders: China (8), India (7), Switzerland (2), United States (1), Taiwan (1), Italy (1).

Do any Liraglutide API holders have FDA warning letters?

Sun Pharmaceutical Industries Ltd has an open FDA warning letter, shown on the listing and in the FDA enforcement tracker.

Does a DMF mean the API is FDA approved?

No. FDA reviews a DMF when a drug application references it and does not approve DMFs on their own.