Suppliers / Tenamyd Pharmaceutical

Tenamyd Pharmaceutical

Vietnam 2 duplicate records merged Updated 9 July 2026

Tenamyd Pharmaceutical is an API and finished-dose manufacturer based in Vietnam. It appears in 183 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
183
filings across 1 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, Vietnam Not on file

What they file, and where

Molecule Regulators Docs
Ceftriaxone DAV (Vietnam) 8
Cefotaxime DAV (Vietnam) 7
Cefoperazone DAV (Vietnam) 6
Ceftizoxime DAV (Vietnam) 6
Cefuroxime DAV (Vietnam) 4
Cefamandole DAV (Vietnam) 3
Cefepime DAV (Vietnam) 3
Cefoxitin DAV (Vietnam) 3
Ceftazidime DAV (Vietnam) 3
Cefalotin DAV (Vietnam) 2
Show all 13 molecules on file
Cefazolin DAV (Vietnam) 2
Cefotiam DAV (Vietnam) 2
Silver Sulfadiazine DAV (Vietnam) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 183 None
EMA None 1

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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