Suppliers / Unijules Life Sciences

Unijules Life Sciences

India 307 employees Updated 9 July 2026

Unijules Life Sciences is a finished-dose manufacturer based in India. It appears in 39 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), EDE (AE) and MINSA (CR). Its GMP standing is certified by NAFDAC (NG). Customs aggregates show $127K of exports covering 12 molecules to 3 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
39
filings across 6 regulators

Registered plants

Site FDA FEI
Nagpur, United Arab Emirates Not on file
Kalmeshwar Dist. Nagpur, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 12 2
EDE (AE) 11 None
MINSA (CR) 6 None
DIGEMAPS (DO) 5 None
NPRA (MY) 3 None
ARCSA (EC) 2 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $671K 10
2025 Not reported $127K 3

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 We do not publish the identity of any buyer.

Questions about Unijules Life Sciences

Does Unijules Life Sciences hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Unijules Life Sciences. It does have 39 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Unijules Life Sciences manufacture?
2 registered sites are on record, in United Arab Emirates and Nigeria (Nagpur and Kalmeshwar Dist. Nagpur). Every site is listed on this page with the register it came from.
Which regulators recognise Unijules Life Sciences's GMP?
Current GMP certificates are on record from NAFDAC (NG). 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
Customs aggregates
Export values, molecule and destination counts