Suppliers / Synokem-Pharmaceuticals-Limited

Synokem-Pharmaceuticals-Limited

India 836 employees 2 duplicate records merged Updated 9 July 2026

Synokem-Pharmaceuticals-Limited is a finished-dose manufacturer based in India. It appears in 93 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with CDSCO (India), UZPHARM (UZ) and NAFDAC (NG). Its GMP standing is certified by NAFDAC (NG) and FDA (GH). Customs aggregates show $3.4M of exports covering 343 molecules to 22 destinations in 2025.

0
active US DMFs
0
valid CEPs
0
registered plants
93
filings across 5 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 73 None
UZPHARM (UZ) 11 None
NAFDAC (NG) 5 1
ARCSA (EC) 2 None
ZAMRA (ZM) 2 None
FDA (GH) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $256K 6
2025 Not reported $3.4M 22
2024 Not reported $2.3M 21
2023 Not reported $2.6M 21

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 We do not publish the identity of any buyer.

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Synokem-Pharmaceuticals-Limited

Does Synokem-Pharmaceuticals-Limited hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Synokem-Pharmaceuticals-Limited. It does have 93 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Synokem-Pharmaceuticals-Limited's GMP?
Current GMP certificates are on record from 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