Suppliers / Reyoung Pharmaceutical

Reyoung Pharmaceutical

China reconciled across 6 public records · 4 entities Updated 9 July 2026

Reyoung Pharmaceutical is an API manufacturer based in China. It holds 9 active US drug master files across a filed portfolio of 9 molecules. Its filings concentrate with ARCSA (EC), DIGEMAPS (DO) and FDA (GH). Its GMP standing is certified by ANVISA (Brazil), MFDS (Korea) and INVIMA (CO), among 7 authorities.

9
active US DMFs
0
valid CEPs
4
registered plants
317
filings across 12 regulators

Registered plants

Site FDA FEI
SHANDONG, China Not on file
Zibo, China Not on file
Shandong, Colombia Not on file
Shandong Province, Nigeria Not on file

What they file, and where

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 79 None
DIGEMAPS (DO) 56 None
FDA (GH) 47 1
NAFDAC (NG) 40 1
MINSA (CR) 31 None
EFDA (ET) 25 None
ANVISA (Brazil) None 4
MFDS (Korea) None 2
INVIMA (CO) None 2
EMA None 2
UZPHARM (UZ) None 2

Questions about Reyoung Pharmaceutical

Does Reyoung Pharmaceutical hold a US DMF or a CEP?
Reyoung Pharmaceutical holds 9 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.
Where does Reyoung Pharmaceutical manufacture?
4 registered sites are on record, in China, Colombia and Nigeria (Shandong, Zibo and Shandong among others). Every site is listed on this page with the register it came from.
What does Reyoung Pharmaceutical make?
9 molecules are on record against Reyoung Pharmaceutical, including Aripiprazole, Avanafil, Avatrombopag and Azilsartan Medoxomil. Each links through to that molecule's full manufacturer list.
Which regulators recognise Reyoung Pharmaceutical's GMP?
Current GMP certificates are on record from ANVISA (Brazil), MFDS (Korea), INVIMA (CO), EMA, UZPHARM (UZ) and 2 more. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates