Suppliers / Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd

Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd

China Updated 9 July 2026

Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd is an API manufacturer based in China. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by MFDS (Korea).

0
active US DMFs
0
valid CEPs
0
registered plants
1
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Metformin SFDA (Saudi Arabia) 2
Gatifloxacin SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Gatifloxacin API Metformin API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None
MFDS (Korea) None 2

Questions about Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd

Does Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd make?
2 molecules are on record against Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd, including Metformin and Gatifloxacin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Huanggang Yinhe Aarti Pharmaceutical Co.,Ltd's GMP?
Current GMP certificates are on record from MFDS (Korea). 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