Suppliers / Dae Han New Pharm

Dae Han New Pharm

South Korea 2 duplicate records merged Updated 9 July 2026

Dae Han New Pharm is a finished-dose manufacturer based in South Korea. It appears in 10 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), ARCSA (EC) and NPRA (MY).

0
active US DMFs
0
valid CEPs
0
registered plants
10
filings across 3 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 7 None
ARCSA (EC) 2 None
NPRA (MY) 1 None

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.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability