Suppliers / Aarti Pharmalabs

Aarti Pharmalabs

India AARTIPHARM.BO Updated 9 July 2026

Aarti Pharmalabs is an API manufacturer based in India. It holds 41 active US drug master files. Its GMP standing is certified by CDSCO (India) and US FDA. Its most recent recorded inspection, by US FDA, closed on 27 March 2026 as VAI. Customs aggregates show $125.7M of exports covering 1,582 molecules to 72 destinations in 2025.

41
active US DMFs
0
valid CEPs
4
registered plants 2 with an FDA FEI number
4
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
5 of 5 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 27 March 2026 VAI US FDA
  • 20 February 2020 VAI US FDA
  • 21 December 2016 VAI US FDA
  • 27 March 2015 VAI US FDA
  • 29 September 2011 VAI US FDA

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

Registered plants

Site FDA FEI
Thane, India 3007005296
Tarapur, India 3005256484
vapi 396 195valsad, India Not on file
Vapi, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 4 None
CDSCO (India) None 2
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $20.1M 44
2025 $242.7M $125.7M 72
2024 $221.4M $89.9M 72
2023 $235.6M $73.5M 70

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Questions about Aarti Pharmalabs

Does Aarti Pharmalabs hold a US DMF or a CEP?
Aarti Pharmalabs holds 41 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Aarti Pharmalabs FDA-registered?
2 sites operated by Aarti Pharmalabs carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Aarti Pharmalabs's last inspection go?
The most recent inspection on record closed on 27 March 2026 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 5 inspections are on file.
Where does Aarti Pharmalabs manufacture?
4 registered sites are on record, in India (Thane, Tarapur and Vapi 396 195valsad among others). Every site is listed on this page with the register it came from.
What does Aarti Pharmalabs make?
30 molecules are on record against Aarti Pharmalabs, including Mometasone Furoate, Fluticasone Propionate, Benazepril and Cyclophosphamide. Each links through to that molecule's full manufacturer list.
Which regulators recognise Aarti Pharmalabs's GMP?
Current GMP certificates are on record from CDSCO (India) and US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was VAI, on 27 March 2026.

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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
Company filings
Revenue as reported