Suppliers / Meyer Organics

Meyer Organics

India Updated 9 July 2026

Meyer Organics is a finished-dose manufacturer based in India. It appears in 90 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with FDA (GH), NAFDAC (NG) and ZAMRA (ZM). Its GMP standing is certified by NAFDAC (NG), CDSCO (India) and FDA (GH). Customs aggregates show $17.9M of exports covering 1,081 molecules to 29 destinations in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants
90
filings across 5 regulators

Registered plants

Site FDA FEI
bengaluru 560 058, India Not on file
Bengaluru Rural, India Not on file
Thane, Nigeria Not on file
Bangalore, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
FDA (GH) 44 2
NAFDAC (NG) 22 4
ZAMRA (ZM) 16 None
MCAZ (ZW) 7 None
UZPHARM (UZ) 1 None
CDSCO (India) None 3

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.1M 14
2025 Not reported $17.9M 29
2024 Not reported $20.9M 31
2023 Not reported $18.9M 29

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 We do not publish the identity of any buyer.

Questions about Meyer Organics

Does Meyer Organics hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Meyer Organics. It does have 90 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Meyer Organics manufacture?
4 registered sites are on record, in India and Nigeria (Bengaluru 560 058, Bengaluru Rural and Thane among others). Every site is listed on this page with the register it came from.
Which regulators recognise Meyer Organics'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