Suppliers / Zhejiang Kingland Pharmaceutical

Zhejiang Kingland Pharmaceutical

China Updated 9 July 2026

Zhejiang Kingland Pharmaceutical is an API manufacturer based in China. It holds 16 active US drug master files across a filed portfolio of 8 molecules.

16
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Alogliptin US FDA 2
Aniracetam US FDA 2
Biotin US FDA 2
Edaravone US FDA 2
Ferric Carboxymaltose US FDA 2
Folic Acid US FDA 2
Ornithine US FDA 2
Riociguat US FDA 2

Also appears on these molecule pages

Alogliptin API Edaravone API Ferric Carboxymaltose API Riociguat API

Questions about Zhejiang Kingland Pharmaceutical

Does Zhejiang Kingland Pharmaceutical hold a US DMF or a CEP?
Zhejiang Kingland Pharmaceutical holds 16 active US drug master files. 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.
What does Zhejiang Kingland Pharmaceutical make?
8 molecules are on record against Zhejiang Kingland Pharmaceutical, including Alogliptin, Aniracetam, Biotin and Edaravone. 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