Suppliers / Ausgenex Pty

Ausgenex Pty

Australia Updated 9 July 2026

Ausgenex Pty is an API manufacturer based in Australia. It holds 3 valid CEPs across a filed portfolio of 3 molecules.

0
active US DMFs
3
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Molendinar, Australia Not on file

What they file, and where

Molecule Regulators Docs
Adult Bovine Serum EDQM 1
Bovine Calf Serum EDQM 1
Foetal Bovine Serum EDQM 1

Also appears on these molecule pages

Foetal Bovine Serum API

Questions about Ausgenex Pty

Does Ausgenex Pty hold a US DMF or a CEP?
Ausgenex Pty holds 3 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.
Where does Ausgenex Pty manufacture?
1 registered site is on record, in Australia (Molendinar). Every site is listed on this page with the register it came from.
What does Ausgenex Pty make?
3 molecules are on record against Ausgenex Pty, including Adult Bovine Serum, Bovine Calf Serum and Foetal Bovine Serum. 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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Sources on this page

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