Suppliers / Rubicon Research

Rubicon Research

India RBCN 3 duplicate records merged Updated 9 July 2026

Rubicon Research is a finished-dose manufacturer based in India. It appears in 32 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA, NPRA (MY) and HSA (SG). Its GMP standing is certified by US FDA, EMA and MFDS (Korea), among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 20 March 2025 as NAI. Customs aggregates show $109.5M of exports covering 2,904 molecules to 9 destinations in 2025.

0
active US DMFs
0
valid CEPs
7
registered plants 4 with an FDA FEI number
32
filings across 8 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
4 of 4 confirmed
Inspections
6 of 6 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 20 March 2025 NAI US FDA
  • 8 March 2024 NAI US FDA
  • 27 January 2023 VAI US FDA
  • 20 November 2017 NAI US FDA
  • 13 March 2015 NAI US FDA
  • 11 April 2013 VAI US FDA

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

Registered plants

Site FDA FEI
Satara, United Arab Emirates Not on file
Satara, India 3012953979
THANE DISTRICT, India Not on file
Thane, India 3008252295
Thane, India 3006559899
Dhar, India 3016480976

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 11 2
NPRA (MY) 9 None
HSA (SG) 6 None
JFDA (JO) 2 None
EDE (AE) 1 None
ARCSA (EC) 1 None
EMA None 2
MFDS (Korea) None 2
MHRA (UK) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $22.2M 4
2025 Not reported $109.5M 9
2024 Not reported $100.8M 8
2023 Not reported $92.1M 9

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 We do not publish the identity of any buyer.

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Open risk flags

  • 18 active litigation matters are on record.
  • The most recent inspection outcome was NAI, on 20 March 2025.

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