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

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Open risk flags

  • The most recent inspection outcome was NAI, on 11 April 2025.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates