Suppliers / Sentiss Pharma

Sentiss Pharma

India 883 employees 2 duplicate records merged Updated 9 July 2026

Sentiss Pharma is a finished-dose manufacturer based in India. It appears in 14 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ) and US FDA. Its GMP standing is certified by EMA and UZPHARM (UZ). Its most recent recorded inspection, by US FDA, closed on 14 May 2019 as OAI. Customs aggregates show $58.8M of exports covering 1,294 molecules to 12 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
14
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 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

  • 14 May 2019 OAI US FDA
  • 23 May 2017 OAI US FDA
  • 29 July 2014 OAI US FDA
  • 3 April 2013 OAI US FDA

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

Registered plants

Site FDA FEI
Solan, India 3008250236
Nalagarh, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 12 1
US FDA 2 None
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $49K 2
2025 Not reported $58.8M 12
2024 Not reported $63.4M 11
2023 Not reported $58.2M 9

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 We do not publish the identity of any buyer.

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Open risk flags

  • The most recent inspection outcome was OAI, on 14 May 2019.

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