Suppliers / Auro Peptides

Auro Peptides

India Updated 9 July 2026

Auro Peptides is an API manufacturer based in India. It holds 14 active US drug master files and 2 valid CEPs across a filed portfolio of 14 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 16 February 2024 as NAI. Customs aggregates show $545K of exports covering 98 molecules to 7 destinations in 2025.

14
active US DMFs
2
valid CEPs
2
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
2 of 2 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 16 February 2024 NAI US FDA
  • 2 September 2016 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Kandi Mandal, India Not on file
Sangareddy District, India 3010923869

What they file, and where

Molecule Regulators Docs
Desmopressin EDQM, US FDA 2
Octreotide EDQM, US FDA 2
Vasopressin SFDA (Saudi Arabia), US FDA 2
Degarelix US FDA 1
Etelcalcetide US FDA 1
Ganirelix US FDA 1
Glatiramer US FDA 1
Icatibant US FDA 1
Leuprolide US FDA 1
Linaclotide US FDA 1
Show all 14 molecules on file
Liraglutide US FDA 1
Plecanatide US FDA 1
Semaglutide US FDA 1
Teriparatide US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $43 2
2025 Not reported $545K 7
2024 Not reported $407K 8
2023 Not reported $2.3M 9

Export figures are customs aggregates. We do not publish the identity of any buyer.

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Open risk flags

  • The most recent inspection outcome was NAI, on 16 February 2024.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts