Suppliers / Liquidia Technologies

Liquidia Technologies

United States Updated 9 July 2026

Liquidia Technologies is a finished-dose manufacturer based in United States. It appears in 4 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
4
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
Morrisville, United States 3008731457

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 4 None

Questions about Liquidia Technologies

Does Liquidia Technologies hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Liquidia Technologies. It does have 4 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Liquidia Technologies FDA-registered?
One site operated by Liquidia 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 Liquidia Technologies manufacture?
1 registered site is on record, in United States (Morrisville). Every site is listed on this page with the register it came from.
Where does Liquidia Technologies file?
Filings are on record with US FDA, 4 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