Suppliers / Sichuan Huiyu Pharmaceutical

Sichuan Huiyu Pharmaceutical

China 53 employees Updated 9 July 2026

Sichuan Huiyu Pharmaceutical is an API and finished-dose manufacturer based in China. It holds 5 active US drug master files across a filed portfolio of 5 molecules. Its filings concentrate with NPRA (MY), UZPHARM (UZ) and MINSA (CR). Its GMP standing is certified by EMA and MHRA (UK).

5
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
20
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Neijiang, United Arab Emirates Not on file
NEIJIANG, China Not on file
Neijiang, China Not on file
China, China 3014500199

What they file, and where

Molecule Regulators Docs
Carfilzomib US FDA 1
Etoposide US FDA 1
Iron Sucrose US FDA 1
Lanreotide US FDA 1
Leucovorin Calcium US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 7 None
UZPHARM (UZ) 6 None
MINSA (CR) 3 None
EDE (AE) 3 None
INVIMA (CO) 1 None
EMA None 3
MHRA (UK) None 1

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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