Suppliers / Verdant Life Sciences

Verdant Life Sciences

India Updated 9 July 2026

Verdant Life Sciences is an API manufacturer based in India. It holds 3 valid CEPs across a filed portfolio of 3 molecules. Its GMP standing is certified by EMA. Customs aggregates show $378K of exports covering 14 molecules to 8 destinations in 2025.

0
active US DMFs
3
valid CEPs
2
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
Anakapalli, India Not on file
Visakhapatnam, India Not on file

What they file, and where

Molecule Regulators Docs
Irbesartan EDQM 1
Sertraline EDQM 1
Telmisartan EDQM 1

Also appears on these molecule pages

Sertraline API Telmisartan API Irbesartan API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $268K 3
2025 Not reported $378K 8

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 We do not publish the identity of any buyer.

Questions about Verdant Life Sciences

Does Verdant Life Sciences hold a US DMF or a CEP?
Verdant Life Sciences holds 3 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 Verdant Life Sciences manufacture?
2 registered sites are on record, in India (Anakapalli and Visakhapatnam). Every site is listed on this page with the register it came from.
What does Verdant Life Sciences make?
3 molecules are on record against Verdant Life Sciences, including Irbesartan, Sertraline and Telmisartan. Each links through to that molecule's full manufacturer list.
Which regulators recognise Verdant Life Sciences'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