Suppliers / Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical

Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical

China Updated 9 July 2026

Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical 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.

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

What they file, and where

Molecule Regulators Docs
Aztreonam SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Aztreonam API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None

Questions about Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical

Does Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical. 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 Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical make?
1 molecule is on record against Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical, including Aztreonam. Each links through to that molecule's full manufacturer list.
Where does Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical file?
Filings are on record with MINSA (CR), 1 in total.

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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability