Suppliers / Suzhou Ryway Biotech

Suzhou Ryway Biotech

China Updated 9 July 2026

Suzhou Ryway Biotech is an API manufacturer based in China. It holds 30 active US drug master files.

30
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
(21R)-Argatroban US FDA 1
Baloxavir Marboxil US FDA 1
Carbimazole US FDA 1
Ceftaroline Fosamil US FDA 1
Distigmine US FDA 1
Dolutegravir US FDA 1
Dotinurad US FDA 1
Ethacridine US FDA 1
Flurbiprofen US FDA 1
Iguratimod US FDA 1
Show all 30 molecules on file
Indobufen US FDA 1
Iodixanol US FDA 1
Iohexol US FDA 1
Iomeprol US FDA 1
Iopamidol US FDA 1
Iopromide US FDA 1
Ioversol US FDA 1
Loxoprofen US FDA 1
Mesna US FDA 1
Metaraminol US FDA 1
Methimazole US FDA 1
Polaprezinc US FDA 1
Propylthiouracil US FDA 1
Semaglutide US FDA 1
Sofosbuvir US FDA 1
Sugammadex US FDA 1
Thymalfasin US FDA 1
Tiopronin US FDA 1
Tirzepatide US FDA 1
Voglibose US FDA 1

Also appears on these molecule pages

Show 5 more molecule pages

Questions about Suzhou Ryway Biotech

Does Suzhou Ryway Biotech hold a US DMF or a CEP?
Suzhou Ryway Biotech holds 30 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 Suzhou Ryway Biotech make?
30 molecules are on record against Suzhou Ryway Biotech, including (21R)-Argatroban, Baloxavir Marboxil, Carbimazole and Ceftaroline Fosamil. 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