Suppliers / Jiangxi Kvvit Pharmaceutical

Jiangxi Kvvit Pharmaceutical

China Updated 9 July 2026

Jiangxi Kvvit Pharmaceutical is an API and finished-dose manufacturer based in China. It holds one active US drug master file.

1
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
1
filings across 1 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
China, China 3037146422

What they file, and where

Molecule Regulators Docs
Enzalutamide US FDA 1

Also appears on these molecule pages

Olaparib finished dose Enzalutamide API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None

Questions about Jiangxi Kvvit Pharmaceutical

Does Jiangxi Kvvit Pharmaceutical hold a US DMF or a CEP?
Jiangxi Kvvit Pharmaceutical holds 1 active US drug master file. 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 Jiangxi Kvvit Pharmaceutical FDA-registered?
One site operated by Jiangxi Kvvit 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.
Where does Jiangxi Kvvit 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 Jiangxi Kvvit Pharmaceutical make?
1 molecule is on record against Jiangxi Kvvit Pharmaceutical, including Enzalutamide. Each links through to that molecule's full manufacturer list.
Where does Jiangxi Kvvit 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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Sources on this page

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