Suppliers / Nira Life Sciences

Nira Life Sciences

India 61 employees Updated 9 July 2026

Nira Life Sciences is an API manufacturer based in India. It holds 2 active US drug master files across a filed portfolio of 2 molecules. Its GMP standing is certified by CDSCO (India). Customs aggregates show $401K of exports covering 22 molecules to 4 destinations in 2025.

2
active US DMFs
0
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Surendranagar, India Not on file

What they file, and where

Molecule Regulators Docs
Benfotiamine US FDA 1
Nitazoxanide US FDA 1

Also appears on these molecule pages

Nitazoxanide API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $338K 3
2025 Not reported $401K 4

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 We do not publish the identity of any buyer.

Questions about Nira Life Sciences

Does Nira Life Sciences hold a US DMF or a CEP?
Nira Life Sciences holds 2 active US drug master files. 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.
Where does Nira Life Sciences manufacture?
1 registered site is on record, in India (Surendranagar). Every site is listed on this page with the register it came from.
What does Nira Life Sciences make?
2 molecules are on record against Nira Life Sciences, including Benfotiamine and Nitazoxanide. Each links through to that molecule's full manufacturer list.
Which regulators recognise Nira Life Sciences's GMP?
Current GMP certificates are on record from CDSCO (India). 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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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