Suppliers / Chieron Active Ingredients

Chieron Active Ingredients

India Updated 9 July 2026

Chieron Active Ingredients is an API manufacturer based in India. It holds 14 active US drug master files across a filed portfolio of 11 molecules. Its most recent recorded inspection, by US FDA, closed on 15 November 2019 as VAI. Customs aggregates show $4.0M of exports covering 120 molecules to 31 destinations in 2025.

14
active US DMFs
0
valid CEPs
1
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

  • 15 November 2019 VAI US FDA
  • 9 June 2017 VAI US FDA

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

Registered plants

Site FDA FEI
Spsr Nellore, India 3006897905

What they file, and where

Molecule Regulators Docs
Olmesartan US FDA 2
Tetracaine US FDA 2
Warfarin US FDA 2
Dapagliflozin US FDA 1
Lacosamide US FDA 1
Levetiracetam US FDA 1
Linagliptin US FDA 1
Risperidone US FDA 1
Rivaroxaban US FDA 1
Sitagliptin US FDA 1
Show all 11 molecules on file
Vildagliptin US FDA 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $2.5M 17
2025 Not reported $4.0M 31

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 We do not publish the identity of any buyer.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 VAI, on 15 November 2019.

Sources on this page

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