Suppliers / Dendron Brands

Dendron Brands

United Kingdom Updated 9 July 2026

Dendron Brands is a finished-dose manufacturer based in United Kingdom. It appears in 17 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, EDE (AE) and MHRA (UK). Its GMP standing is certified by MHRA (UK), MFDS (Korea) and ANVISA (Brazil), among 4 authorities.

0
active US DMFs
0
valid CEPs
2
registered plants
17
filings across 7 regulators

Registered plants

Site FDA FEI
Hertfordshire, United Arab Emirates Not on file
WATFORD, United Kingdom Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 8 None
EDE (AE) 3 None
MHRA (UK) 2 3
ARCSA (EC) 1 None
EDA (EG) 1 None
DIGEMAPS (DO) 1 None
MFDS (Korea) None 2
ANVISA (Brazil) None 2
NCELS (KZ) None 1

Questions about Dendron Brands

Does Dendron Brands hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dendron Brands. It does have 17 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dendron Brands manufacture?
2 registered sites are on record, in United Arab Emirates and United Kingdom (Hertfordshire and Watford). Every site is listed on this page with the register it came from.
Which regulators recognise Dendron Brands's GMP?
Current GMP certificates are on record from MHRA (UK), MFDS (Korea), ANVISA (Brazil) and NCELS (KZ). 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