Suppliers / Nitin Lifesciences

Nitin Lifesciences

India 212 employees Updated 9 July 2026

Nitin Lifesciences is a finished-dose manufacturer based in India. It appears in 49 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), NPRA (MY) and ARCSA (EC). Its GMP standing is certified by NAFDAC (NG), CDSCO (India) and FDA (GH). Customs aggregates show $3.9M of exports covering 161 molecules to 8 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
49
filings across 5 regulators

Registered plants

Site FDA FEI
karnal 132001, India Not on file
Sirmour, Nigeria Not on file
Pin, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 23 3
NPRA (MY) 10 None
ARCSA (EC) 8 None
UZPHARM (UZ) 5 None
DIGEMAPS (DO) 3 None
CDSCO (India) None 2
FDA (GH) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $727K 2
2025 Not reported $3.9M 8
2024 Not reported $1.2M 8
2023 Not reported $1.3M 7

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 We do not publish the identity of any buyer.

Questions about Nitin Lifesciences

Does Nitin Lifesciences hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Nitin Lifesciences. It does have 49 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Nitin Lifesciences manufacture?
3 registered sites are on record, in India and Nigeria (Karnal 132001, Sirmour and Pin). Every site is listed on this page with the register it came from.
Which regulators recognise Nitin Lifesciences's GMP?
Current GMP certificates are on record from NAFDAC (NG), CDSCO (India) and FDA (GH). 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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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