Suppliers / Kreative Organics

Kreative Organics

India 69 employees Updated 9 July 2026

Kreative Organics is an API manufacturer based in India. It holds 8 active US drug master files and 4 valid CEPs across a filed portfolio of 10 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 2 May 2025 as VAI. Customs aggregates show $4.8M of exports covering 76 molecules to 20 destinations in 2025.

8
active US DMFs
4
valid CEPs
1
registered plants 1 with an FDA FEI number
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 2 May 2025 VAI US FDA
  • 7 February 2020 VAI US FDA
  • 14 April 2017 OAI US FDA
  • 2 May 2014 OAI US FDA

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

Registered plants

Site FDA FEI
Hyderabad, India 3003447972

What they file, and where

Molecule Regulators Docs
Bisacodyl EDQM, US FDA 2
Etodolac EDQM, US FDA 2
Choline Salicylate US FDA 1
Diclofenac US FDA 1
Ferric Carboxymaltose US FDA 1
Glipizide US FDA 1
Hydroxyzine EDQM 1
Methenamine US FDA 1
Salsalate US FDA 1
Sodium Picosulfate EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 1 None
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $586K 9
2025 Not reported $4.8M 20
2024 Not reported $4.1M 27
2023 Not reported $4.7M 21

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 We do not publish the identity of any buyer.

Questions about Kreative Organics

Does Kreative Organics hold a US DMF or a CEP?
Kreative Organics holds 8 active US drug master files and 4 valid CEPs. 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 Kreative Organics FDA-registered?
One site operated by Kreative Organics carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Kreative Organics's last inspection go?
The most recent inspection on record closed on 2 May 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 4 inspections are on file, of which 2 closed as OAI.
Where does Kreative Organics manufacture?
1 registered site is on record, in India (Hyderabad). Every site is listed on this page with the register it came from.
What does Kreative Organics make?
10 molecules are on record against Kreative Organics, including Bisacodyl, Etodolac, Choline Salicylate and Diclofenac. Each links through to that molecule's full manufacturer list.
Which regulators recognise Kreative Organics's GMP?
Current GMP certificates are on record from 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 2 May 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