Suppliers / MSN Life Sciences

MSN Life Sciences

India 2 duplicate records merged Updated 9 July 2026

The public registers hold a second record for MSN Life Sciences. The fuller profile, with 517 active US DMFs and 121 valid CEPs, is at MSN Laboratories. Figures on this page cover only this record.

MSN Life Sciences is an API and finished-dose manufacturer based in India. It holds 160 active US drug master files and 48 valid CEPs. Its filings concentrate with ARCSA (EC), CDSCO (India) and MINSA (CR). Its GMP standing is certified by EMA, MFDS (Korea) and US FDA. Its most recent recorded inspection, by US FDA, closed on 13 September 2024 as VAI. Customs aggregates show $9.6M of exports covering 198 molecules to 34 destinations in 2025.

160
active US DMFs
48
valid CEPs
6
registered plants 2 with an FDA FEI number
84
filings across 4 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
3 of 3 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

  • 13 September 2024 VAI US FDA
  • 3 June 2022 VAI US FDA
  • 30 June 2017 VAI US FDA

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

Registered plants

Site FDA FEI
Chandampet Village, India Not on file
Medak District, India 3011543392
Bhiknoor Village, India Not on file
Medak, India Not on file
Kamareddy, India Not on file
Kamareddy District, India 3014775167

What they file, and where

Molecule Regulators Docs
Esomeprazole EDQM, SFDA (Saudi Arabia), US FDA 7
Sacubitril SFDA (Saudi Arabia), US FDA 6
Sitagliptin EDQM, SFDA (Saudi Arabia), US FDA 5
Apremilast US FDA 4
Macitentan SFDA (Saudi Arabia), US FDA 4
Mebendazole EDQM, US FDA 4
Metoprolol EDQM, US FDA 4
Pirfenidone EDQM, SFDA (Saudi Arabia), US FDA 4
Riociguat EDQM, SFDA (Saudi Arabia), US FDA 4
Darunavir SFDA (Saudi Arabia), US FDA 3
Show all 30 molecules on file
Empagliflozin SFDA (Saudi Arabia), US FDA 3
Haloperidol EDQM, US FDA 3
Levetiracetam EDQM, SFDA (Saudi Arabia), US FDA 3
Losartan EDQM, SFDA (Saudi Arabia), US FDA 3
Albendazole EDQM, US FDA 2
Atorvastatin SFDA (Saudi Arabia), US FDA 2
Bupivacaine EDQM, US FDA 2
Canagliflozin US FDA 2
Caspofungin SFDA (Saudi Arabia), US FDA 2
Clobazam EDQM, US FDA 2
Clopidogrel US FDA 2
Desvenlafaxine US FDA 2
Dolutegravir US FDA 2
Doxepin EDQM, US FDA 2
Elvitegravir US FDA 2
Famotidine EDQM, US FDA 2
Flecainide EDQM, US FDA 2
Fluphenazine US FDA 2
Gadobutrol EDQM, US FDA 2
Glimepiride EDQM, US FDA 2

Also appears on these molecule pages

Show 101 more molecule pages
Carbidopa API Carfilzomib finished dose Caspofungin API Chlorthalidone API Clobazam API Clopidogrel API Cobicistat API Crisaborole API Dabigatran Etexilate API Dabigatran Etexilate Mesilate API Daclatasvir API Darunavir API Dasatinib finished dose Desvenlafaxine API Deutetrabenazine API Difelikefalin API Dofetilide API Dolutegravir API Doxepin API Droxidopa API Edoxaban API Elagolix API Eluxadoline API Elvitegravir API Empagliflozin API Eslicarbazepine API Esomeprazole API Etelcalcetide API Exenatide API Famotidine API Favipiravir API Ferric Carboxymaltose API Finerenone API Flecainide API Fluphenazine API Gadobutrol API Glimepiride API Haloperidol API Haloperidol Decanoate API Hydroxychloroquine API Icatibant API Irbesartan API Isavuconazonium API Istradefylline API Letermovir API Levetiracetam API Levodopa API Levofloxacin API Levomilnacipran API Lifitegrast API Linaclotide API Lisinopril API Losartan API Macitentan API Mebendazole API Mesalamine API Mesalazine API Metformin API Metolazone API Metoprolol API Micafungin API Mirabegron finished dose Nitazoxanide API Obeticholic Acid API Oseltamivir API Oxcarbazepine API Pantoprazole API Penicillamine API Pimavanserin API Pirfenidone API Plecanatide API Pomalidomide finished dose Pregabalin API Ranolazine API Regadenoson API Rimegepant API Riociguat API Rosuvastatin API Rufinamide API Sacubitril API Safinamide API Semaglutide API Silodosin finished dose Sitagliptin API Sucralfate API Sugammadex API Tavaborole API Teduglutide API Tenofovir Alafenamide API Tenofovir Disoproxil API Teriparatide API Tirzepatide API Trazodone API Valsartan API Venlafaxine API Vericiguat API Vigabatrin API Vonoprazan API Voxelotor API Zavegepant API Ziprasidone API

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 45 None
CDSCO (India) 22 None
MINSA (CR) 9 None
INVIMA (CO) 8 None
EMA None 2
MFDS (Korea) None 2
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $8.0M 30
2025 Not reported $9.6M 34

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

Questions about MSN Life Sciences

Does MSN Life Sciences hold a US DMF or a CEP?
MSN Life Sciences holds 160 active US drug master files and 48 valid CEPs. 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 MSN Life Sciences FDA-registered?
2 sites operated by MSN Life Sciences carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did MSN Life Sciences's last inspection go?
The most recent inspection on record closed on 13 September 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file.
Where does MSN Life Sciences manufacture?
6 registered sites are on record, in India (Chandampet Village, Medak District and Bhiknoor Village among others). Every site is listed on this page with the register it came from.
What does MSN Life Sciences make?
30 molecules are on record against MSN Life Sciences, including Esomeprazole, Sacubitril, Sitagliptin and Apremilast. Each links through to that molecule's full manufacturer list.
Which regulators recognise MSN Life Sciences's GMP?
Current GMP certificates are on record from EMA, MFDS (Korea) and US FDA. 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

  • 15 active litigation matters are on record.
  • The most recent inspection outcome was VAI, on 13 September 2024.

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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