Suppliers / Hanlim Pharmaceutical

Hanlim Pharmaceutical

United States 2 duplicate records merged Updated 9 July 2026

Hanlim Pharmaceutical is a finished-dose manufacturer based in United States. It appears in 20 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), NPRA (MY) and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
0
registered plants
20
filings across 5 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 10 None
NPRA (MY) 4 None
NAFDAC (NG) 2 None
NMPA (CN) 2 None
UZPHARM (UZ) 2 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