Suppliers / Novacyl SAS

Novacyl SAS

France 2 duplicate records merged Updated 9 July 2026

Novacyl SAS is an API manufacturer based in France. It holds 4 active US drug master files across a filed portfolio of 2 molecules. Its GMP standing is certified by ANSM (FR).

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

Registered plants

Site FDA FEI
SAINT FONS, France Not on file
ROUSSILLON, France Not on file
St Fons, France Not on file
Roussillon, France Not on file

What they file, and where

Molecule Regulators Docs
Acetylsalicylic Acid SFDA (Saudi Arabia), US FDA 5
Salicylic Acid SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Acetylsalicylic Acid API Salicylic Acid API

Filings and GMP by regulator

Regulator Filings GMP certificates
ANSM (FR) None 46

Scale

Year Revenue Exports Destinations
2024 $131.2M 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 We do not publish the identity of any buyer.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 Novacyl SAS

Does Novacyl SAS hold a US DMF or a CEP?
Novacyl SAS holds 4 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.
Where does Novacyl SAS manufacture?
4 registered sites are on record, in France (Saint Fons, Roussillon and St Fons among others). Every site is listed on this page with the register it came from.
What does Novacyl SAS make?
2 molecules are on record against Novacyl SAS, including Acetylsalicylic Acid and Salicylic Acid. Each links through to that molecule's full manufacturer list.
Which regulators recognise Novacyl SAS's GMP?
Current GMP certificates are on record from ANSM (FR). 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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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