Suppliers / Medinex Laboratories

Medinex Laboratories

India 27 employees Updated 9 July 2026

Medinex Laboratories is an API manufacturer based in India. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India). Customs aggregates show $637K of exports covering 14 molecules to 9 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
1
filings across 1 regulators

Registered plants

Site FDA FEI
Mumbai, India Not on file
tehsil ghogha ukharala bhavnagar, India Not on file
tehsil ghoghaukharlabha vnagar, India Not on file

What they file, and where

Molecule Regulators Docs
Norepinephrine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Norepinephrine API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None
CDSCO (India) None 3

Scale

Year Revenue Exports Destinations
2025 Not reported $637K 9

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 We do not publish the identity of any buyer.

Questions about Medinex Laboratories

Does Medinex Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Medinex Laboratories. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Medinex Laboratories manufacture?
3 registered sites are on record, in India (Mumbai, Tehsil Ghogha Ukharala Bhavnagar and Tehsil Ghoghaukharlabha Vnagar). Every site is listed on this page with the register it came from.
What does Medinex Laboratories make?
1 molecule is on record against Medinex Laboratories, including Norepinephrine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Medinex Laboratories'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