Suppliers / Medreich

Medreich

India 2 duplicate records merged Updated 9 July 2026

Medreich is a finished-dose manufacturer based in India. It appears in 198 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with MEDSAFE (NZ), NAFDAC (NG) and EMA. Its GMP standing is certified by EMA, MHRA (UK) and CDSCO (India), among 5 authorities. Customs aggregates show $157.7M of exports covering 3,969 molecules to 49 destinations in 2025.

0
active US DMFs
0
valid CEPs
8
registered plants
198
filings across 11 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
FELTHAM, United Kingdom Not on file
hoskote taluk bengaluru rural, India Not on file
bengaluru 62, India Not on file
BANGALORE RURAL DISTRICT, India Not on file
Bangaluru, India Not on file
Bengaluru Rural, India Not on file

2 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
MEDSAFE (NZ) 58 None
NAFDAC (NG) 48 4
EMA 27 6
DH (HK) 23 None
ARCSA (EC) 18 None
MINSA (CR) 8 None
MHRA (UK) None 5
CDSCO (India) None 4
FDA (GH) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $24.2M 29
2025 Not reported $157.7M 49
2024 Not reported $169.2M 47
2023 Not reported $163.4M 58

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 We do not publish the identity of any buyer.

Questions about Medreich

Does Medreich hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Medreich. It does have 198 filings with 11 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Medreich manufacture?
8 registered sites are on record, in United Kingdom, India and Nigeria (Feltham, Hoskote Taluk Bengaluru Rural and Bengaluru 62 among others). Every site is listed on this page with the register it came from.
Which regulators recognise Medreich's GMP?
Current GMP certificates are on record from EMA, MHRA (UK), CDSCO (India), NAFDAC (NG) 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