Suppliers / ESJAY Pharma

ESJAY Pharma

India 176 employees 2 duplicate records merged Updated 9 July 2026

ESJAY Pharma is a finished-dose manufacturer based in India. It appears in 5 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by EMA. Customs aggregates show $6.9M of exports covering 121 molecules to 1 destination in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants 2 with an FDA FEI number
5
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Kancheepuram, India 3027393896
Kanchipuram, India Not on file
East Windsor, United States 3012257624

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 5 None
EMA None 1

Scale

Year Revenue Exports Destinations
2025 Not reported $6.9M 1
2024 Not reported $204K 1

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 We do not publish the identity of any buyer.

Questions about ESJAY Pharma

Does ESJAY Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for ESJAY Pharma. It does have 5 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is ESJAY Pharma FDA-registered?
2 sites operated by ESJAY Pharma 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.
Where does ESJAY Pharma manufacture?
3 registered sites are on record, in India and United States (Kancheepuram, Kanchipuram and East Windsor). Every site is listed on this page with the register it came from.
Which regulators recognise ESJAY Pharma'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