Suppliers / Phil Inter Pharma

Phil Inter Pharma

Vietnam Updated 9 July 2026

Phil Inter Pharma is an API and finished-dose manufacturer based in Vietnam. It appears in 339 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), RAMA (GE) and UZPHARM (UZ). Its GMP standing is certified by MHRA (UK) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
339
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
HO CHI MINH CITY, Vietnam Not on file
Ho Chi Minh, Vietnam Not on file

What they file, and where

Molecule Regulators Docs
L-Ornithin L-Aspartat DAV (Vietnam) 5
Cefotaxime DAV (Vietnam) 4
Ursodeoxycholic Acid DAV (Vietnam) 4
Cefdinir DAV (Vietnam) 2
Cefixime DAV (Vietnam) 2
Cefpirome DAV (Vietnam) 2
Cefuroxime DAV (Vietnam) 2
Aceclofenac DAV (Vietnam) 1
Alverine DAV (Vietnam) 1
Cefazolin DAV (Vietnam) 1
Show all 24 molecules on file
Cefepime DAV (Vietnam) 1
Ceftazidime DAV (Vietnam) 1
Ceftriaxone DAV (Vietnam) 1
Chondroitin Sulfate DAV (Vietnam) 1
Cystein DAV (Vietnam) 1
Dutasteride DAV (Vietnam) 1
Ferrous DAV (Vietnam) 1
Fusidic Acid DAV (Vietnam) 1
Ibuprofen DAV (Vietnam) 1
Myrtol DAV (Vietnam) 1
Nystatin DAV (Vietnam) 1
Simethicon DAV (Vietnam) 1
Sulbactam DAV (Vietnam) 1
Tretinoin DAV (Vietnam) 1

Also appears on these molecule pages

Adapalene finished dose Alverine API Calci finished dose Cefaclor finished dose Cefadroxil contract manufacturing Cefazolin API Cefdinir API Cefepime API Cefixime API Cefoperazone contract manufacturing Cefotaxime API Cefoxitin finished dose
Show 17 more molecule pages
Cefprozil finished dose Ceftazidime contract manufacturing Ceftriaxone API Cefuroxime API Dexibuprofen finished dose Dutasteride API Econazole finished dose Ferrous API Fusidic Acid API Ibuprofen API L-Ornithin L-Aspartat API Neomycin contract manufacturing Nystatin API Simethicon API Sulbactam contract manufacturing Tretinoin API Ursodeoxycholic Acid API

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 335 None
RAMA (GE) 2 None
UZPHARM (UZ) 2 None
MHRA (UK) None 2
EMA None 2

Questions about Phil Inter Pharma

Does Phil Inter Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Phil Inter Pharma. It does have 339 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Phil Inter Pharma manufacture?
2 registered sites are on record, in Vietnam (HO CHI Minh City and Ho Chi Minh). Every site is listed on this page with the register it came from.
What does Phil Inter Pharma make?
24 molecules are on record against Phil Inter Pharma, including L-Ornithin L-Aspartat, Cefotaxime, Ursodeoxycholic Acid and Cefdinir. Each links through to that molecule's full manufacturer list.
Which regulators recognise Phil Inter Pharma's GMP?
Current GMP certificates are on record from MHRA (UK) and EMA. 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