Suppliers / Jubilant Life Sciences

Jubilant Life Sciences

India Updated 9 July 2026

Jubilant Life Sciences is an API manufacturer based in India. It appears in 19 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada and DIGEMAPS (DO).

0
active US DMFs
0
valid CEPs
0
registered plants
19
filings across 2 regulators

What they file, and where

Molecule Regulators Docs
Atorvastatin SFDA (Saudi Arabia) 1
Citalopram SFDA (Saudi Arabia) 1
Esomeprazole SFDA (Saudi Arabia) 1
Lamotrigine SFDA (Saudi Arabia) 1
Oxcarbazepine SFDA (Saudi Arabia) 1
Pantoprazole SFDA (Saudi Arabia) 1
Quetiapine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Citalopram API Oxcarbazepine API Atorvastatin API Quetiapine API Esomeprazole API Pantoprazole API Lamotrigine API

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 17 None
DIGEMAPS (DO) 2 None

Questions about Jubilant Life Sciences

Does Jubilant Life Sciences hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Jubilant Life Sciences. It does have 19 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
What does Jubilant Life Sciences make?
7 molecules are on record against Jubilant Life Sciences, including Atorvastatin, Citalopram, Esomeprazole and Lamotrigine. Each links through to that molecule's full manufacturer list.
Where does Jubilant Life Sciences file?
Filings are on record with Health Canada and DIGEMAPS (DO), 19 in total.

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

Jubilant Biosys shares 2 molecules Apitoria Pharma shares 1 molecule Hetero shares 1 molecule Cipla shares 1 molecule Dr Reddy's Laboratories shares 1 molecule

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