Suppliers / Naxpar Pharma

Naxpar Pharma

India 127 employees 2 duplicate records merged Updated 9 July 2026

Naxpar Pharma is a finished-dose manufacturer based in India. It appears in 18 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), CDSCO (India) and NAFDAC (NG). Its GMP standing is certified by CDSCO (India) and NAFDAC (NG). Customs aggregates show $22K of exports covering 1 molecule to 1 destination in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants
18
filings across 5 regulators

Registered plants

Site FDA FEI
Dist.Solan, United Arab Emirates Not on file
sura t 394 230surat, India Not on file
G.I.D.C., India Not on file
Baddi, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 7 None
CDSCO (India) 4 2
NAFDAC (NG) 3 1
MINSA (CR) 3 None
EDE (AE) 1 None

Scale

Year Revenue Exports Destinations
2025 Not reported $22K 1
2024 Not reported $13K 1
2023 Not reported $40K 2
2022 Not reported $584K 3

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 We do not publish the identity of any buyer.

Questions about Naxpar Pharma

Does Naxpar Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Naxpar Pharma. It does have 18 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Naxpar Pharma manufacture?
4 registered sites are on record, in United Arab Emirates, India and Nigeria (Dist.solan, Sura T 394 230surat and G.i.d.c. among others). Every site is listed on this page with the register it came from.
Which regulators recognise Naxpar Pharma's GMP?
Current GMP certificates are on record from CDSCO (India) and NAFDAC (NG). 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