Suppliers / SNJ Labs

SNJ Labs

India 48 employees Updated 9 July 2026

SNJ Labs is an API manufacturer based in India. It holds 8 active US drug master files and one valid CEP across a filed portfolio of 7 molecules. Its GMP standing is certified by CDSCO (India).

8
active US DMFs
1
valid CEPs
3
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
Dist. Rajkot, India Not on file
Padavala, India 3026587575
padavalara jkot, India Not on file

What they file, and where

Molecule Regulators Docs
Pirfenidone EDQM, US FDA 2
Sucralfate US FDA 2
Clotrimazole US FDA 1
Desvenlafaxine US FDA 1
Ferric Carboxymaltose US FDA 1
Iron US FDA 1
Sucrose US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Questions about SNJ Labs

Does SNJ Labs hold a US DMF or a CEP?
SNJ Labs holds 8 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 SNJ Labs FDA-registered?
One site operated by SNJ Labs 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 SNJ Labs manufacture?
3 registered sites are on record, in India (Dist. Rajkot, Padavala and Padavalara Jkot). Every site is listed on this page with the register it came from.
What does SNJ Labs make?
7 molecules are on record against SNJ Labs, including Pirfenidone, Sucralfate, Clotrimazole and Desvenlafaxine. Each links through to that molecule's full manufacturer list.
Which regulators recognise SNJ Labs's GMP?
Current GMP certificates are on record from CDSCO (India). 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates