Suppliers / Shandong Luning Pharmaceutical

Shandong Luning Pharmaceutical

China Updated 9 July 2026

Shandong Luning Pharmaceutical is an API manufacturer based in China. It holds 3 active US drug master files and one valid CEP across a filed portfolio of 3 molecules.

3
active US DMFs
1
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Dongying City, China Not on file

What they file, and where

Molecule Regulators Docs
Lipoic Acid EDQM, US FDA 2
Alogliptin US FDA 1
Tadalafil US FDA 1

Also appears on these molecule pages

Alogliptin API Lipoic Acid API Tadalafil API

Questions about Shandong Luning Pharmaceutical

Does Shandong Luning Pharmaceutical hold a US DMF or a CEP?
Shandong Luning Pharmaceutical holds 3 active US drug master files and 1 valid CEP. 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 Shandong Luning Pharmaceutical manufacture?
1 registered site is on record, in China (Dongying City). Every site is listed on this page with the register it came from.
What does Shandong Luning Pharmaceutical make?
3 molecules are on record against Shandong Luning Pharmaceutical, including Lipoic Acid, Alogliptin and Tadalafil. Each links through to that molecule's full manufacturer list.

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