Suppliers / Ningxia Hengkang Technology

Ningxia Hengkang Technology

China Updated 9 July 2026

Ningxia Hengkang Technology is an API manufacturer based in China. It holds 2 active US drug master files and 2 valid CEPs across a filed portfolio of 2 molecules.

2
active US DMFs
2
valid CEPs
2
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
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Yinchuan, China Not on file
China, China 3013336231

What they file, and where

Molecule Regulators Docs
Metformin EDQM, US FDA 3
Metformin Hydrochloride EDQM 1

Also appears on these molecule pages

Metformin API

Questions about Ningxia Hengkang Technology

Does Ningxia Hengkang Technology hold a US DMF or a CEP?
Ningxia Hengkang Technology holds 2 active US drug master files and 2 valid CEPs. 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 Ningxia Hengkang Technology FDA-registered?
One site operated by Ningxia Hengkang Technology 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.
Where does Ningxia Hengkang Technology manufacture?
2 registered sites are on record, in China (Yinchuan and China). Every site is listed on this page with the register it came from.
What does Ningxia Hengkang Technology make?
2 molecules are on record against Ningxia Hengkang Technology, including Metformin and Metformin Hydrochloride. Each links through to that molecule's full manufacturer list.

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