Suppliers / India Glycols

India Glycols

India Updated 9 July 2026

India Glycols is an API manufacturer based in India. It holds 2 active US drug master files and 2 valid CEPs across a filed portfolio of 3 molecules. Its GMP standing is certified by EMA. Customs aggregates show $26.1M of exports covering 744 molecules to 42 destinations in 2025.

2
active US DMFs
2
valid CEPs
1
registered plants
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Dehradun, India Not on file

What they file, and where

Molecule Regulators Docs
Nicotine US FDA 2
Colchicine EDQM 1
Thiocolchicoside Crystallised From Ethanol EDQM 1

Also appears on these molecule pages

Colchicine API Nicotine API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $6.5M 23
2025 Not reported $26.1M 42
2024 Not reported $24.8M 46
2023 Not reported $41.3M 46

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 We do not publish the identity of any buyer.

Questions about India Glycols

Does India Glycols hold a US DMF or a CEP?
India Glycols holds 2 active US drug master files and 2 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.
Where does India Glycols manufacture?
1 registered site is on record, in India (Dehradun). Every site is listed on this page with the register it came from.
What does India Glycols make?
3 molecules are on record against India Glycols, including Nicotine, Colchicine and Thiocolchicoside Crystallised From Ethanol. Each links through to that molecule's full manufacturer list.
Which regulators recognise India Glycols's GMP?
Current GMP certificates are on record from EMA. 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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

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