Suppliers / Blue Zone Technologies

Blue Zone Technologies

Canada 10 employees Updated 9 July 2026

Blue Zone Technologies is an API manufacturer based in Canada. It holds 2 active US drug master files across a filed portfolio of 2 molecules.

2
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Canada, Canada 3006192191

What they file, and where

Molecule Regulators Docs
Desflurane US FDA 1
Sevoflurane US FDA 1

Also appears on these molecule pages

Sevoflurane API

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 1 None

Questions about Blue Zone Technologies

Does Blue Zone Technologies hold a US DMF or a CEP?
Blue Zone Technologies 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.
Is Blue Zone Technologies FDA-registered?
One site operated by Blue Zone Technologies 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.
Where does Blue Zone Technologies manufacture?
1 registered site is on record, in Canada (Canada). Every site is listed on this page with the register it came from.
What does Blue Zone Technologies make?
2 molecules are on record against Blue Zone Technologies, including Desflurane and Sevoflurane. Each links through to that molecule's full manufacturer list.
Where does Blue Zone Technologies file?
Filings are on record with Health Canada, 1 in total.

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