Givinostat Hydrochloride
Who holds supplier records for Givinostat Hydrochloride? 2 organisations hold a current record for Givinostat Hydrochloride: an active US FDA Type II Drug Master File. Recorded organisation countries for current records: Italy (1); not recorded for 1.
Sources: FDA Drug Master File list, EDQM certification database, FDA Orange Book. Record updated 4 Aug 2026. How we read these records
Reading the evidence
- 2 current records
Several organisations hold current DMFs or CEPs. Whether any is a usable source for your grade, scale and market still needs qualification.
- 1 with a company-level GMP certificate on record
These organisations have at least one current EU or UK GMP certificate somewhere. It is not matched to the site that makes this substance; check the certificate's site and scope.
Current records (2)
Organisations holding an active US FDA Type II Drug Master File or a CEP for Givinostat Hydrochloride. Country is the organisation's recorded country, not necessarily the manufacturing site.
- BEIJING HOPE PHARMACEUTICAL CO LTDActive DMF 44405 · latest filing Jun 2026
- CHEMI SPAItaly Company GMP cert on recordActive DMF 37344 · latest filing Apr 2023
The Sourcing Desk contacts candidates, confirms current supply, grade and site, and screens each against its regulatory record, for a buyer-paid fixed fee and never a supplier commission.
Overview
Givinostat Hydrochloride is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL6068400).
Chemical identity
- IUPAC name
- [6-(diethylaminomethyl)naphthalen-2-yl]methyl N-[4-(hydroxycarbamoyl)phenyl]carbamate;hydrate;hydrochloride
- Canonical SMILES
- CCN(CC)CC1=CC2=C(C=C1)C=C(C=C2)COC(=O)NC3=CC=C(C=C3)C(=O)NO.O.Cl
- InChIKey
- FKGKZBBDJSKCIS-UHFFFAOYSA-N
- Synonyms
- Duvyzat, Givinostat hydrochloride, ITF2357 HYDROCHLORIDE, ITF-2357 HYDROCHLORIDE MONOHYDRATE, ITF2357 HYDROCHLORIDE MONOHYDRATE, Givinostat Hydrochloride Hydrate, RefChem:639979, Givinostat hydrochloride monohydrate, Givinostat (ITF2357), Givinostat (hydrochloride monohydrate), ITF2357 (Givinostat), Givinostat hydrochloride (USAN)
Record history
PharmaTek records which organisations hold a current DMF or CEP for Givinostat Hydrochloride every week, starting 23 Oct 2026. Additions and lapses will appear here from the next weekly release.
Monitoring pilot: get an email when these records change. Places are confirmed by a person; nothing is sent until then. All changes this week
What these records establish
- An active DMF means a confidential file is held by the FDA and can be referenced; the FDA does not approve or disapprove DMFs.
- A CEP confirms monograph suitability for the EU market; it is not a GMP certificate, and the holder may not be the manufacturer.
- Historical records show a past filing, not current supply.
- Company GMP certificates are matched to the organisation, not to the site making this substance.
- A substance missing from these registers is not evidence that no supplier exists.
Frequently asked questions
Which organisations hold current supplier records for Givinostat Hydrochloride?
2 organisations hold an active US FDA Type II Drug Master File or a CEP for Givinostat Hydrochloride: BEIJING HOPE PHARMACEUTICAL CO LTD and CHEMI SPA (Italy). A DMF or CEP shows a regulatory filing, not current commercial availability, and the holder is not necessarily the manufacturing site.
Which Givinostat Hydrochloride Drug Master Files are active?
BEIJING HOPE PHARMACEUTICAL CO LTD (DMF 44405) and CHEMI SPA (DMF 37344). The FDA does not approve or disapprove DMFs; an active DMF can be referenced in an application once its holder issues a letter of authorisation.
How do I qualify a Givinostat Hydrochloride supplier?
Confirm the DMF or CEP is current and covers your grade, obtain the letter of authorisation, identify the actual manufacturing site and check its GMP certificate and FDA inspection history, audit the site or review a recent audit, and run comparable requests for information across more than one candidate.
Do you supply Givinostat Hydrochloride?
Send a link to a certificate, registration or filing we have missed or got wrong. We check it against the issuing register before changing anything; information we cannot check against a register is shown as supplier-reported.