Suppliers / Phytex Australia

Phytex Australia

Australia 14 employees Updated 9 July 2026

Phytex Australia is an API manufacturer based in Australia. It holds 2 active US drug master files across a filed portfolio of 2 molecules.

2
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Methscopolamine Bromide US FDA 1
Scopolamine US FDA 1

Also appears on these molecule pages

Questions about Phytex Australia

Does Phytex Australia hold a US DMF or a CEP?
Phytex Australia holds 2 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.
What does Phytex Australia make?
2 molecules are on record against Phytex Australia, including Methscopolamine Bromide and 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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Sources on this page

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