Peptide API Manufacturers in India

16 companies are listed as peptide API manufacturers in India. 16 hold active US Drug Master Files for peptide APIs, most often for Semaglutide, Icatibant, Liraglutide. 14 have a regulator record of GMP manufacturing. 11 score High (90 or more). 3 listings carry an open FDA warning letter, which caps the score at 60.

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

Peptide API Manufacturers in India (16)

High
GMP

Vadodara drug maker, dating to 1907, with three API plants and six formulation plants. Holds US DMFs for 6 peptide APIs, including glatiramer and tirzepatide.

Model
Manufacturer
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping
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
FDC Limited
Mumbai, India
High
GMP

Mumbai drugmaker founded in 1936 with six plants, including a US-FDA-accredited API site at Roha; holds an active US DMF for semaglutide.

Model
Manufacturer
Manufacturer?
Yes
GMP CertifiedUS-FDA Accredited SiteUS DMF HolderIn-House Production
Gland Pharma Ltd
Hyderabad, India
High
GMP

Hyderabad injectables CDMO founded 1978, promoted by Fosun Pharma; FDA-inspected sites; US DMF for glatiramer acetate.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleCDMO
GMP

Hyderabad-based MSN Group entity holding US DMFs for 11 peptide APIs, including semaglutide and tirzepatide. MSN runs 27 plants in India, the USA and Indonesia.

Model
CDMO
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
Neuland Laboratories
Hyderabad, India
High
GMPCOA

Indian API manufacturer and CDMO with a peptide synthesis platform.

Model
CDMO
Manufacturer?
Yes
GMP CertifiedIn-House ProductionInternational Shipping
GMP

Hyderabad API developer and maker founded in 2007, focused on niche and complex products. Holds US DMFs for cetrorelix, icatibant and sincalide.

Model
Manufacturer
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping
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
Hetero Drugs Ltd
Hyderabad, India
Medium

Privately held Hyderabad generics and API group with 36+ plants; US DMFs for semaglutide and vasopressin.

Model
Manufacturer
Manufacturer?
Yes
In-House ProductionWholesale
Medium

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

Model
Manufacturer
Manufacturer?
Yes
In-House ProductionWholesale
Cipla Ltd
Mumbai, India
Low
GMP

Mumbai drug maker incorporated in 1935 with plants in India and the USA. Holds US DMFs for difelikefalin, icatibant and terlipressin. Pithampur FDA warning letter still open.

Notice: open regulatory issue
Model
Manufacturer
Manufacturer?
Yes
GMP CertifiedIn-House ProductionWholesaleInternational Shipping
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
USV Private Limited
Mumbai, India
Low
GMP

Mumbai drug maker with its own API and formulation plants in India. Holds US DMFs for 3 peptide APIs. Received an FDA CGMP warning letter in November 2026.

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

More in India

Peptide APIs with US DMFs held by companies in India

Peptide API Manufacturers in other countries

Frequently asked questions

How many peptide API manufacturers in India are listed?

16 companies. Each listing shows location, business model, documentation and a score from 0 to 100.

Which peptide API manufacturers in India score highest?

By score: Alembic Pharmaceuticals Ltd (98), Auro Peptides Ltd (98), Biocon Ltd (98), FDC Limited (98), Gland Pharma Ltd (98). Scores measure checkable evidence, not product quality, and paid placement does not change them.

Which peptide API manufacturers in India hold US Drug Master Files?

Alembic Pharmaceuticals Ltd, Auro Peptides Ltd, Biocon Ltd, FDC Limited, Gland Pharma Ltd, MSN Life Sciences Private Ltd (MSN Group), Piramal Pharma Ltd (Piramal Pharma Solutions), Shilpa Pharma Lifesciences Ltd, Neuland Laboratories, Biophore India Pharmaceuticals Pvt Ltd and 6 more hold active Type II DMFs for peptide APIs in FDA's DMF list. A DMF is a confidential file submitted to FDA; FDA does not approve DMFs, but drug applications can reference them.

How should I check a supplier before ordering?

Confirm the legal entity, ask for lot-specific certificates of analysis that the testing lab can verify, check FDA warning letters and import alerts, and for GMP material ask for regulator inspection records rather than marketing claims.