Suppliers / Lunan Better Pharmaceutical

Lunan Better Pharmaceutical

China Updated 9 July 2026

Lunan Better Pharmaceutical is an API and finished-dose manufacturer based in China. It holds one active US drug master file. Its filings concentrate with ARCSA (EC), MINSA (CR) and UZPHARM (UZ). Its GMP standing is certified by EAEU_EEC and NAFDAC (NG).

1
active US DMFs
0
valid CEPs
1
registered plants
6
filings across 4 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
0 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Shandong Province, Nigeria Not on file

What they file, and where

Molecule Regulators Docs
Zolpidem US FDA 1

Also appears on these molecule pages

Isoflurane finished dose Sevoflurane finished dose Tirofiban finished dose Zolpidem API

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 2 None
MINSA (CR) 2 None
UZPHARM (UZ) 1 None
DIGEMAPS (DO) 1 None
EAEU_EEC None 1
NAFDAC (NG) None 1

Questions about Lunan Better Pharmaceutical

Does Lunan Better Pharmaceutical hold a US DMF or a CEP?
Lunan Better Pharmaceutical holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Lunan Better Pharmaceutical manufacture?
1 registered site is on record, in Nigeria (Shandong Province). Every site is listed on this page with the register it came from.
What does Lunan Better Pharmaceutical make?
1 molecule is on record against Lunan Better Pharmaceutical, including Zolpidem. Each links through to that molecule's full manufacturer list.
Which regulators recognise Lunan Better Pharmaceutical's GMP?
Current GMP certificates are on record from EEC (Eurasian Economic Union) and NAFDAC (NG). 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates