Suppliers / Shandong Guobang Pharmaceutical

Shandong Guobang Pharmaceutical

China 6 employees Updated 9 July 2026

The public registers hold a second record for Shandong Guobang Pharmaceutical. The fuller profile, with 16 active US DMFs and 15 valid CEPs, is at Zhejiang Guobang. Figures on this page cover only this record.

Shandong Guobang Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file and 2 valid CEPs. Its GMP standing is certified by MFDS (Korea).

1
active US DMFs
2
valid CEPs
2
registered plants 1 with an FDA FEI number
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Weifang, China Not on file
China, China 3002946929

What they file, and where

Molecule Regulators Docs
Doxycycline EDQM, US FDA 3

Also appears on these molecule pages

Doxycycline API

Filings and GMP by regulator

Regulator Filings GMP certificates
FDA (GH) 1 None
MFDS (Korea) None 2

Questions about Shandong Guobang Pharmaceutical

Does Shandong Guobang Pharmaceutical hold a US DMF or a CEP?
Shandong Guobang Pharmaceutical holds 1 active US drug master file and 2 valid CEPs. 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.
Is Shandong Guobang Pharmaceutical FDA-registered?
One site operated by Shandong Guobang Pharmaceutical carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Shandong Guobang Pharmaceutical manufacture?
2 registered sites are on record, in China (Weifang and China). Every site is listed on this page with the register it came from.
What does Shandong Guobang Pharmaceutical make?
1 molecule is on record against Shandong Guobang Pharmaceutical, including Doxycycline. Each links through to that molecule's full manufacturer list.
Which regulators recognise Shandong Guobang Pharmaceutical's GMP?
Current GMP certificates are on record from MFDS (Korea). 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