Suppliers / Phytex Australia Pty

Phytex Australia Pty

Australia Updated 9 July 2026

Phytex Australia Pty is an API manufacturer based in Australia. It holds one valid CEP.

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

Registered plants

Site FDA FEI
Peakhurst, Australia Not on file

What they file, and where

Molecule Regulators Docs
Scopolamine EDQM 1

Also appears on these molecule pages

Scopolamine API

Questions about Phytex Australia Pty

Does Phytex Australia Pty hold a US DMF or a CEP?
Phytex Australia Pty holds 1 valid CEP. 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 Phytex Australia Pty manufacture?
1 registered site is on record, in Australia (Peakhurst). Every site is listed on this page with the register it came from.
What does Phytex Australia Pty make?
1 molecule is on record against Phytex Australia Pty, including Scopolamine. 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