Suppliers / Jubilant Pharmova

Jubilant Pharmova

India Updated 9 July 2026

Jubilant Pharmova is an API manufacturer based in India. It holds 4 active US drug master files across a filed portfolio of 6 molecules. Its filings concentrate with MINSA (CR) and NCELS (KZ). Its GMP standing is certified by CDSCO (India). Customs aggregates show $39.0M of exports covering 448 molecules to 46 destinations in 2025.

4
active US DMFs
0
valid CEPs
1
registered plants
5
filings across 2 regulators

Registered plants

Site FDA FEI
Mysuru, India Not on file

What they file, and where

Molecule Regulators Docs
Olanzapine SFDA (Saudi Arabia), US FDA 2
Dalfampridine US FDA 1
Donepezil SFDA (Saudi Arabia) 1
Lansoprazole US FDA 1
Meclizine US FDA 1
Sitagliptin SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Dalfampridine API Lansoprazole API Meclizine API Olanzapine API Sitagliptin API Donepezil API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 4 None
NCELS (KZ) 1 None
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $120K 1
2025 Not reported $39.0M 46
2024 Not reported $41.8M 45
2023 Not reported $62.2M 46

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 We do not publish the identity of any buyer.

Questions about Jubilant Pharmova

Does Jubilant Pharmova hold a US DMF or a CEP?
Jubilant Pharmova holds 4 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.
Where does Jubilant Pharmova manufacture?
1 registered site is on record, in India (Mysuru). Every site is listed on this page with the register it came from.
What does Jubilant Pharmova make?
6 molecules are on record against Jubilant Pharmova, including Olanzapine, Dalfampridine, Donepezil and Lansoprazole. Each links through to that molecule's full manufacturer list.
Which regulators recognise Jubilant Pharmova'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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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