Suppliers / Shandong Qidu Pharmaceutical Co.,Ltd

Shandong Qidu Pharmaceutical Co.,Ltd

China Updated 9 July 2026

Shandong Qidu Pharmaceutical Co.,Ltd is a finished-dose manufacturer based in China. It appears in 22 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), MINSA (CR) and NAFDAC (NG). Its GMP standing is certified by MFDS (Korea), NAFDAC (NG) and UZPHARM (UZ).

0
active US DMFs
0
valid CEPs
1
registered plants
22
filings across 5 regulators

Registered plants

Site FDA FEI
LINZI DISTRICT, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 12 1
MINSA (CR) 5 None
NAFDAC (NG) 2 1
ARCSA (EC) 2 None
DIGEMAPS (DO) 1 None
MFDS (Korea) None 2

Questions about Shandong Qidu Pharmaceutical Co.,Ltd

Does Shandong Qidu Pharmaceutical Co.,Ltd hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Shandong Qidu Pharmaceutical Co.,Ltd. It does have 22 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Shandong Qidu Pharmaceutical Co.,Ltd manufacture?
1 registered site is on record, in Nigeria (Linzi District). Every site is listed on this page with the register it came from.
Which regulators recognise Shandong Qidu Pharmaceutical Co.,Ltd's GMP?
Current GMP certificates are on record from MFDS (Korea), NAFDAC (NG) and UZPHARM (UZ). 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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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