Suppliers / Jubilant Generics

Jubilant Generics

India 855 employees Updated 9 July 2026

Jubilant Generics is an API and finished-dose manufacturer based in India. It appears in 166 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA, Health Canada and MINSA (CR). Its GMP standing is certified by MHRA (UK), US FDA and NAFDAC (NG), among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 2 February 2024 as VAI. Customs aggregates show $36.7M of exports covering 1,283 molecules to 44 destinations in 2025.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
166
filings across 10 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
8 of 8 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 2 February 2024 VAI US FDA
  • 1 August 2022 OAI US FDA
  • 12 March 2021 OAI US FDA
  • 6 November 2019 OAI US FDA
  • 23 March 2017 NAI US FDA
  • 8 April 2016 VAI US FDA
  • 13 March 2015 VAI US FDA
  • 1 March 2013 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Uttarakhand, United Arab Emirates Not on file
Roorkee, United Arab Emirates Not on file
UTTARAKHAND, India Not on file
HARIDWAR, India Not on file
Roorkee, India 3006895982

What they file, and where

Molecule Regulators Docs
Risperidone SFDA (Saudi Arabia) 2
Solifenacin Succinate SFDA (Saudi Arabia) 2
Aripiprazole SFDA (Saudi Arabia) 1
Deferasirox SFDA (Saudi Arabia) 1
Escitalopram SFDA (Saudi Arabia) 1
Esomeprazole SFDA (Saudi Arabia) 1
Irbesartan SFDA (Saudi Arabia) 1
Lacosamide SFDA (Saudi Arabia) 1
Olanzapine SFDA (Saudi Arabia) 1
Quetiapine SFDA (Saudi Arabia) 1
Show all 13 molecules on file
Tadalafil SFDA (Saudi Arabia) 1
Valsartan SFDA (Saudi Arabia) 1
Zolmitriptan SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Amantadine finished dose Azithromycin finished dose Bumetanide finished dose Bupropion finished dose Citalopram finished dose Clonidine finished dose Darifenacin finished dose Deferasirox API Escitalopram API Eslicarbazepine finished dose Felodipine finished dose Indomethacin finished dose
Show 17 more molecule pages
Lacosamide API Lurasidone finished dose Olanzapine API Olmesartan Medoxomil finished dose Oseltamivir finished dose Ranolazine finished dose Risperidone API Rizatriptan finished dose Solifenacin API Tizanidine finished dose Zolmitriptan API Valsartan API Quetiapine API Esomeprazole API Tadalafil API Irbesartan API Aripiprazole API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 95 1
Health Canada 32 None
MINSA (CR) 14 None
CDSCO (India) 7 None
EDE (AE) 6 None
NMRC (NA) 5 None
MHRA (UK) None 1
NAFDAC (NG) None 1
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.7M 20
2025 Not reported $36.7M 44
2024 Not reported $33.5M 35
2023 Not reported $37.6M 39

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

Questions about Jubilant Generics

Does Jubilant Generics hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Jubilant Generics. It does have 166 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Jubilant Generics FDA-registered?
One site operated by Jubilant Generics 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.
How did Jubilant Generics's last inspection go?
The most recent inspection on record closed on 2 February 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file, of which 3 closed as OAI.
Where does Jubilant Generics manufacture?
5 registered sites are on record, in United Arab Emirates and India (Uttarakhand, Roorkee and Uttarakhand among others). Every site is listed on this page with the register it came from.
What does Jubilant Generics make?
13 molecules are on record against Jubilant Generics, including Risperidone, Solifenacin Succinate, Aripiprazole and Deferasirox. Each links through to that molecule's full manufacturer list.
Which regulators recognise Jubilant Generics's GMP?
Current GMP certificates are on record from MHRA (UK), US FDA, NAFDAC (NG) and EMA. 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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Open risk flags

  • 10 active litigation matters are on record.
  • The most recent inspection outcome was VAI, on 2 February 2024.

Comparable suppliers

Apitoria Pharma shares 7 molecules Hetero shares 5 molecules Dr Reddy's Laboratories shares 5 molecules Cipla shares 4 molecules Alivus Life Sciences shares 4 molecules

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