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

Questions about Lotus Pharmaceutical

Does Lotus Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Lotus Pharmaceutical. It does have 75 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Lotus Pharmaceutical manufacture?
2 registered sites are on record, in United Arab Emirates and Taiwan (Nantou City and Nantou). Every site is listed on this page with the register it came from.
Which regulators recognise Lotus Pharmaceutical's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and EMA. 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

Bora Pharmaceutical Laboratories also in Taiwan Bora Pharmaceuticals also in Taiwan Lotus Pharmaceutical Co Ltd Nantou Plant also in Taiwan Nang Kuang Pharmaceutical also in Taiwan Tty Biopharm also in Taiwan

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