Suppliers / Devi Pharmatech

Devi Pharmatech

India 32 employees Updated 9 July 2026

Devi Pharmatech is an API manufacturer based in India. It holds 2 active US drug master files and one valid CEP across a filed portfolio of 3 molecules. Customs aggregates show $609K of exports covering 15 molecules to 5 destinations in 2025.

2
active US DMFs
1
valid CEPs
2
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Visakhapatnam, India Not on file
Vishakapatnam, India 3030450565

What they file, and where

Molecule Regulators Docs
Bezafibrate EDQM 1
Ruxolitinib US FDA 1
Triheptanoin US FDA 1

Also appears on these molecule pages

Bezafibrate API Ruxolitinib API Triheptanoin API

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $302K 1
2025 Not reported $609K 5
2024 Not reported $19K 2
2023 Not reported $3K 1

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 We do not publish the identity of any buyer.

Questions about Devi Pharmatech

Does Devi Pharmatech hold a US DMF or a CEP?
Devi Pharmatech holds 2 active US drug master files and 1 valid CEP. 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 Devi Pharmatech FDA-registered?
One site operated by Devi Pharmatech 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.
Where does Devi Pharmatech manufacture?
2 registered sites are on record, in India (Visakhapatnam and Vishakapatnam). Every site is listed on this page with the register it came from.
What does Devi Pharmatech make?
3 molecules are on record against Devi Pharmatech, including Bezafibrate, Ruxolitinib and Triheptanoin. Each links through to that molecule's full manufacturer list.

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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Comparable suppliers

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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
Customs aggregates
Export values, molecule and destination counts