Suppliers / Kumar Organic Products

Kumar Organic Products

India Updated 9 July 2026

Kumar Organic Products is an API manufacturer based in India. It holds 5 active US drug master files across a filed portfolio of 3 molecules. Its GMP standing is certified by CDSCO (India) and US FDA. Its most recent recorded inspection, by US FDA, closed on 22 August 2025 as VAI. Customs aggregates show $21.8M of exports covering 677 molecules to 53 destinations in 2025.

5
active US DMFs
0
valid CEPs
7
registered plants 3 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
3 of 3 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 22 August 2025 VAI US FDA
  • 13 June 2025 VAI US FDA
  • 21 April 2023 VAI US FDA
  • 14 November 2019 OAI US FDA
  • 8 February 2019 VAI US FDA
  • 20 July 2018 NAI US FDA
  • 22 September 2016 VAI US FDA
  • 13 May 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
Hassan, India Not on file
Vadodara, India 3009167769
Hassan, India 3008957541
hassan 573 201, India Not on file
Bangalore, India 3003768909
Bengaluru, India Not on file

1 further sites are on record.

What they file, and where

Molecule Regulators Docs
Ciclopirox US FDA 3
Minoxidil SFDA (Saudi Arabia), US FDA 3
Triclosan US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

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

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.5M 31
2025 Not reported $21.8M 53
2024 Not reported $17.1M 50
2023 Not reported $18.7M 46

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 We do not publish the identity of any buyer.

Questions about Kumar Organic Products

Does Kumar Organic Products hold a US DMF or a CEP?
Kumar Organic Products holds 5 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 Kumar Organic Products FDA-registered?
3 sites operated by Kumar Organic Products 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 Kumar Organic Products's last inspection go?
The most recent inspection on record closed on 22 August 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file, of which 1 closed as OAI.
Where does Kumar Organic Products manufacture?
7 registered sites are on record, in India (Hassan, Vadodara and Hassan 573 201 among others). Every site is listed on this page with the register it came from.
What does Kumar Organic Products make?
3 molecules are on record against Kumar Organic Products, including Ciclopirox, Minoxidil and Triclosan. Each links through to that molecule's full manufacturer list.
Which regulators recognise Kumar Organic Products'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 22 August 2025.

Comparable suppliers

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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