Suppliers / MSN Life Sciences

MSN Life Sciences

India 2 duplicate records merged Updated 9 July 2026

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 MFDS (Korea), EMA 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
Kamareddy, India Not on file
Bhiknoor Village, India Not on file
Medak, India Not on file
Medak District, India 3011543392
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 27 more molecule pages

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
MFDS (Korea) None 2
EMA 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.

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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.

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