Suppliers / JQC (Huayin) Pharmaceutical

JQC (Huayin) Pharmaceutical

China Updated 9 July 2026

JQC (Huayin) Pharmaceutical is an API manufacturer based in China. It holds 3 active US drug master files across a filed portfolio of 3 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 17 January 2025 as NAI.

3
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 17 January 2025 NAI US FDA
  • 9 December 2016 VAI US FDA
  • 24 January 2013 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
China, China 3005139325

What they file, and where

Molecule Regulators Docs
Acetylsalicylic Acid US FDA 1
Methyl Salicylate US FDA 1
Salicylic Acid US FDA 1

Also appears on these molecule pages

Acetylsalicylic Acid API Salicylic Acid API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about JQC (Huayin) Pharmaceutical

Does JQC (Huayin) Pharmaceutical hold a US DMF or a CEP?
JQC (Huayin) Pharmaceutical holds 3 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.
Is JQC (Huayin) Pharmaceutical FDA-registered?
One site operated by JQC (Huayin) Pharmaceutical carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did JQC (Huayin) Pharmaceutical's last inspection go?
The most recent inspection on record closed on 17 January 2025 as NAI (No Action Indicated: nothing objectionable was found). 3 inspections are on file.
Where does JQC (Huayin) Pharmaceutical manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does JQC (Huayin) Pharmaceutical make?
3 molecules are on record against JQC (Huayin) Pharmaceutical, including Acetylsalicylic Acid, Methyl Salicylate and Salicylic Acid. Each links through to that molecule's full manufacturer list.
Which regulators recognise JQC (Huayin) Pharmaceutical's GMP?
Current GMP certificates are on record from US FDA. 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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Open risk flags

  • The most recent inspection outcome was NAI, on 17 January 2025.

Comparable suppliers

Novacyl SAS shares 2 molecules Hebei Jingye Medical Technology shares 2 molecules Zydus Lifesciences shares 1 molecule Shandong Xinhua Pharmaceutical shares 1 molecule The Andhra Sugars shares 1 molecule

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
EudraGMDP and national regulators
GMP certificates