Suppliers / Sydler Remedies

Sydler Remedies

India Updated 9 July 2026

Sydler Remedies is a finished-dose manufacturer based in India. It appears in 31 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with EEC_EAEU, MINSA (CR) and DIGEMAPS (DO). Its GMP standing is certified by FDA (GH), EMA and NAFDAC (NG). Customs aggregates show $3.8M of exports covering 290 molecules to 21 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
31
filings across 6 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
MAHARASHTA, United Arab Emirates Not on file
Pune, India Not on file
Maharashtra India, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EEC_EAEU 12 None
MINSA (CR) 10 None
DIGEMAPS (DO) 6 None
MCAZ (ZW) 1 None
EDE (AE) 1 None
UZPHARM (UZ) 1 None
FDA (GH) None 1
EMA None 1
NAFDAC (NG) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $560K 12
2025 Not reported $3.8M 21
2024 Not reported $3.6M 23
2023 Not reported $5.3M 23

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 We do not publish the identity of any buyer.

Questions about Sydler Remedies

Does Sydler Remedies hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sydler Remedies. It does have 31 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sydler Remedies manufacture?
3 registered sites are on record, in United Arab Emirates, India and Nigeria (Maharashta, Pune and Maharashtra India). Every site is listed on this page with the register it came from.
Which regulators recognise Sydler Remedies's GMP?
Current GMP certificates are on record from FDA (GH), EMA 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