Suppliers / SK Chemicals

SK Chemicals

South Korea 2 duplicate records merged Updated 9 July 2026

SK Chemicals is a finished-dose manufacturer based in South Korea. It appears in 11 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with NMPA (CN), SFDA (Saudi Arabia) and EMA. Its GMP standing is certified by EMA and ANVISA (Brazil). Customs aggregates show $473 of exports covering 2 molecules to 1 destination in 2022.

0
active US DMFs
0
valid CEPs
2
registered plants
11
filings across 5 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
CHEONGJU, South Korea Not on file
Cheongju-Si, South Korea Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NMPA (CN) 4 None
SFDA (Saudi Arabia) 3 None
EMA 2 2
EDA (EG) 1 None
DIGEMAPS (DO) 1 None
ANVISA (Brazil) None 1

Scale

Year Revenue Exports Destinations
2022 Not reported $473 1

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 We do not publish the identity of any buyer.

Questions about SK Chemicals

Does SK Chemicals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for SK Chemicals. It does have 11 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does SK Chemicals manufacture?
2 registered sites are on record, in South Korea (Cheongju and Cheongju-si). Every site is listed on this page with the register it came from.
Which regulators recognise SK Chemicals's GMP?
Current GMP certificates are on record from EMA and ANVISA (Brazil). 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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Comparable suppliers

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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