Suppliers / Công ty TNHH US Pharma USA

Công ty TNHH US Pharma USA

Vietnam Updated 9 July 2026

Công ty TNHH US Pharma USA is an API and finished-dose manufacturer based in Vietnam. It appears in 29 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
29
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Cefpodoxime DAV (Vietnam) 3
Cefaclor DAV (Vietnam) 2
Thiocolchicoside DAV (Vietnam) 2
Carbimazole DAV (Vietnam) 1
Cefdinir DAV (Vietnam) 1
Cefixime DAV (Vietnam) 1
Clarithromycin DAV (Vietnam) 1
Colchicine DAV (Vietnam) 1
Eperisone DAV (Vietnam) 1
Esomeprazole DAV (Vietnam) 1
Show all 16 molecules on file
Etodolac DAV (Vietnam) 1
Etoricoxib DAV (Vietnam) 1
Montelukast DAV (Vietnam) 1
Racecadotril DAV (Vietnam) 1
Spiramycin DAV (Vietnam) 1
Valsartan DAV (Vietnam) 1

Also appears on these molecule pages

Show 5 more molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 29 None

Questions about Công ty TNHH US Pharma USA

Does Công ty TNHH US Pharma USA hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Công ty TNHH US Pharma USA. It does have 29 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Công ty TNHH US Pharma USA make?
16 molecules are on record against Công ty TNHH US Pharma USA, including Cefpodoxime, Cefaclor, Thiocolchicoside and Carbimazole. Each links through to that molecule's full manufacturer list.
Where does Công ty TNHH US Pharma USA file?
Filings are on record with DAV (Vietnam), 29 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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Sources on this page

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