Suppliers / Shandong Guobang Pharmaceutical

Shandong Guobang Pharmaceutical

China 6 employees Updated 9 July 2026

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

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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