Suppliers / Phoenix Pharma

Phoenix Pharma

Dominican Republic 11 employees 2 duplicate records merged Updated 9 July 2026

Phoenix Pharma is a finished-dose manufacturer based in Dominican Republic. It appears in 184 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), EDA (EG) and NAFDAC (NG). Its GMP standing is certified by ZLG (DE).

0
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
184
filings across 4 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
Hanau, Germany Not on file
Dominican Republic, Dominican Republic 3014491256

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 167 None
EDA (EG) 12 None
NAFDAC (NG) 4 None
FDA (GH) 1 None
ZLG (DE) None 2

Questions about Phoenix Pharma

Does Phoenix Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Phoenix Pharma. It does have 184 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Phoenix Pharma FDA-registered?
One site operated by Phoenix Pharma 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 Phoenix Pharma manufacture?
2 registered sites are on record, in Germany and Dominican Republic (Hanau and Dominican Republic). Every site is listed on this page with the register it came from.
Which regulators recognise Phoenix Pharma's GMP?
Current GMP certificates are on record from ZLG (DE). 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