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

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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