Suppliers / Suraj Laboratories

Suraj Laboratories

India 128 employees Updated 9 July 2026

Suraj Laboratories is an API manufacturer based in India. It holds 2 active US drug master files across a filed portfolio of 2 molecules. Customs aggregates show $66K of exports covering 22 molecules to 3 destinations in 2025.

2
active US DMFs
0
valid CEPs
1
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
Yadgir, India 3030355960

What they file, and where

Molecule Regulators Docs
Aripiprazole US FDA 1
Fenofibrate US FDA 1

Also appears on these molecule pages

Fenofibrate API Aripiprazole API

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $36K 1
2025 Not reported $66K 3

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 We do not publish the identity of any buyer.

Questions about Suraj Laboratories

Does Suraj Laboratories hold a US DMF or a CEP?
Suraj Laboratories holds 2 active US drug master files. 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 Suraj Laboratories FDA-registered?
One site operated by Suraj Laboratories 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 Suraj Laboratories manufacture?
1 registered site is on record, in India (Yadgir). Every site is listed on this page with the register it came from.
What does Suraj Laboratories make?
2 molecules are on record against Suraj Laboratories, including Aripiprazole and Fenofibrate. 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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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