Suppliers / Công ty TNHH United International Pharma

Công ty TNHH United International Pharma

Vietnam Updated 9 July 2026

Công ty TNHH United International Pharma is an API manufacturer based in Vietnam. It appears in 81 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
81
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Ibuprofen DAV (Vietnam) 2
Metformin DAV (Vietnam) 2
Valsartan DAV (Vietnam) 2
Aluminum Hydroxide DAV (Vietnam) 1
Ambroxol DAV (Vietnam) 1
Amlodipine DAV (Vietnam) 1
Ascorbic Acid DAV (Vietnam) 1
Attapulgite DAV (Vietnam) 1
Cholecalciferol DAV (Vietnam) 1
Dextrose DAV (Vietnam) 1
Show all 12 molecules on file
Losartan DAV (Vietnam) 1
Trimetazidine DAV (Vietnam) 1

Also appears on these molecule pages

Ambroxol API Trimetazidine API Ibuprofen API Amlodipine API Valsartan API Metformin API Losartan API

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 81 None

Questions about Công ty TNHH United International Pharma

Does Công ty TNHH United International Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Công ty TNHH United International Pharma. It does have 81 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Công ty TNHH United International Pharma make?
12 molecules are on record against Công ty TNHH United International Pharma, including Ibuprofen, Metformin, Valsartan and Aluminum Hydroxide. Each links through to that molecule's full manufacturer list.
Where does Công ty TNHH United International Pharma file?
Filings are on record with DAV (Vietnam), 81 in total.

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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Comparable suppliers

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability