Suppliers / Jazz Pharmaceuticals

Jazz Pharmaceuticals

Ireland Updated 9 July 2026

Jazz Pharmaceuticals is a finished-dose manufacturer based in Ireland. It appears in 101 regulatory filings across 16 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, EMA and AIFA (IT). Its GMP standing is certified by MHRA (UK).

0
active US DMFs
0
valid CEPs
4
registered plants
101
filings across 16 regulators

Registered plants

Site FDA FEI
D04 E5W7, United Arab Emirates Not on file
Zug, Switzerland Not on file
SITTINGBOURNE, United Kingdom Not on file
Sintra, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 26 None
EMA 13 None
AIFA (IT) 12 None
FAMHP (BE) 8 None
US FDA 8 None
SWISSMEDIC (CH) 6 None
MHRA (UK) None 6

Scale

Year Revenue Exports Destinations
2024 $3.4M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Questions about Jazz Pharmaceuticals

Does Jazz Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Jazz Pharmaceuticals. It does have 101 filings with 16 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Jazz Pharmaceuticals manufacture?
4 registered sites are on record, in United Arab Emirates, Switzerland, United Kingdom and Portugal (D04 E5w7, Zug and Sittingbourne among others). Every site is listed on this page with the register it came from.
Which regulators recognise Jazz Pharmaceuticals's GMP?
Current GMP certificates are on record from MHRA (UK). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates
Company filings
Revenue as reported