Suppliers / Viyash Life Sciences

Viyash Life Sciences

India 2 duplicate records merged Updated 9 July 2026

Viyash Life Sciences is an API manufacturer based in India. It holds 21 active US drug master files and 9 valid CEPs across a filed portfolio of 26 molecules. Its GMP standing is certified by US FDA and EMA. Its most recent recorded inspection, by US FDA, closed on 25 April 2025 as VAI. Customs aggregates show $1.4M of exports covering 22 molecules to 12 destinations in 2025.

21
active US DMFs
9
valid CEPs
3
registered plants 2 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
6 of 6 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

  • 25 April 2025 VAI US FDA
  • 16 February 2024 VAI US FDA
  • 16 October 2018 VAI US FDA
  • 16 November 2017 NAI US FDA
  • 17 July 2015 VAI US FDA
  • 6 March 2012 VAI US FDA

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

Registered plants

Site FDA FEI
Hyderabad, India Not on file
Raigad, India 3003908605
Visakhapatnam, India 3008652704

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 2
EMA None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $338K 5
2025 Not reported $1.4M 12

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 We do not publish the identity of any buyer.

Questions about Viyash Life Sciences

Does Viyash Life Sciences hold a US DMF or a CEP?
Viyash Life Sciences holds 21 active US drug master files and 9 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 Viyash Life Sciences FDA-registered?
2 sites operated by Viyash 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 Viyash Life Sciences's last inspection go?
The most recent inspection on record closed on 25 April 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 6 inspections are on file.
Where does Viyash Life Sciences manufacture?
3 registered sites are on record, in India (Hyderabad, Raigad and Visakhapatnam). Every site is listed on this page with the register it came from.
What does Viyash Life Sciences make?
26 molecules are on record against Viyash Life Sciences, including Baclofen, Labetalol, Lacosamide and Losartan. Each links through to that molecule's full manufacturer list.
Which regulators recognise Viyash Life Sciences's GMP?
Current GMP certificates are on record from US FDA 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

  • The most recent inspection outcome was VAI, on 25 April 2025.

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