Suppliers / zhejiang xianju pharmaceutical

zhejiang xianju pharmaceutical

China 002332.SZ 146 employees Updated 9 July 2026

zhejiang xianju pharmaceutical is an API manufacturer based in China. It holds 22 active US drug master files across a filed portfolio of 19 molecules.

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

What they file, and where

Molecule Regulators Docs
Dexamethasone SFDA (Saudi Arabia), US FDA 3
Prednisolone SFDA (Saudi Arabia), US FDA 3
Testosterone US FDA 3
Methylprednisolone SFDA (Saudi Arabia), US FDA 2
Rocuronium SFDA (Saudi Arabia), US FDA 2
Betamethasone US FDA 1
Brexanolone US FDA 1
Estradiol US FDA 1
Ethinylestradiol US FDA 1
Hydrocortisone US FDA 1
Show all 19 molecules on file
Levonorgestrel US FDA 1
Medroxyprogesterone Acetate US FDA 1
Megestrol Acetate US FDA 1
Mifepristone US FDA 1
Prednisone US FDA 1
Progesterone US FDA 1
Tiotropium US FDA 1
Triamcinolone US FDA 1
Vecuronium US FDA 1

Also appears on these molecule pages

Show 5 more molecule pages

Questions about zhejiang xianju pharmaceutical

Does zhejiang xianju pharmaceutical hold a US DMF or a CEP?
zhejiang xianju pharmaceutical holds 22 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 xianju pharmaceutical make?
19 molecules are on record against zhejiang xianju pharmaceutical, including Dexamethasone, Prednisolone, Testosterone and Methylprednisolone. 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