Suppliers / Evonik Rexim (Nanning) Pharmaceutical

Evonik Rexim (Nanning) Pharmaceutical

China Updated 9 July 2026

Evonik Rexim (Nanning) Pharmaceutical is an API manufacturer based in China. It holds 5 active US drug master files across a filed portfolio of 6 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 11 April 2025 as NAI.

5
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

  • 11 April 2025 NAI US FDA
  • 28 September 2018 VAI US FDA
  • 13 November 2015 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 3004268442

What they file, and where

Molecule Regulators Docs
Aspartic Acid SFDA (Saudi Arabia), US FDA 3
Alanine SFDA (Saudi Arabia), US FDA 2
Glycine SFDA (Saudi Arabia), US FDA 2
Methionine SFDA (Saudi Arabia), US FDA 2
Leucine US FDA 1
Valine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Alanine API Aspartic Acid API Leucine API Methionine API Valine API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about Evonik Rexim (Nanning) Pharmaceutical

Does Evonik Rexim (Nanning) Pharmaceutical hold a US DMF or a CEP?
Evonik Rexim (Nanning) Pharmaceutical holds 5 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 Evonik Rexim (Nanning) Pharmaceutical FDA-registered?
One site operated by Evonik Rexim (Nanning) 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 Evonik Rexim (Nanning) Pharmaceutical's last inspection go?
The most recent inspection on record closed on 11 April 2025 as NAI (No Action Indicated: nothing objectionable was found). 3 inspections are on file.
Where does Evonik Rexim (Nanning) 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 Evonik Rexim (Nanning) Pharmaceutical make?
6 molecules are on record against Evonik Rexim (Nanning) Pharmaceutical, including Aspartic Acid, Alanine, Glycine and Methionine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Evonik Rexim (Nanning) 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 11 April 2025.

Comparable suppliers

Amino Chemicals shares 5 molecules Ajinomoto shares 4 molecules Kyowa Hakko Bio shares 4 molecules Shanghai Plumino Amino Acid shares 4 molecules Shijiazhuang Jirong Pharmaceutical shares 2 molecules

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