Suppliers / Lotus Pharmaceutical

Lotus Pharmaceutical

Taiwan 2 employees Updated 9 July 2026

Lotus Pharmaceutical is a finished-dose manufacturer based in Taiwan. It appears in 75 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by ANVISA (Brazil) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
75
filings across 1 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
Nantou City, United Arab Emirates Not on file
NANTOU, Taiwan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DH (HK) 75 None
ANVISA (Brazil) None 3
EMA None 1

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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