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

Show 2 more molecule pages

Filings and GMP by regulator

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

Questions about Tenamyd Pharmaceutical

Does Tenamyd Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Tenamyd Pharmaceutical. It does have 183 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Tenamyd Pharmaceutical manufacture?
1 registered site is on record, in Vietnam (Ho Chi Minh). Every site is listed on this page with the register it came from.
What does Tenamyd Pharmaceutical make?
13 molecules are on record against Tenamyd Pharmaceutical, including Ceftriaxone, Cefotaxime, Cefoperazone and Ceftizoxime. Each links through to that molecule's full manufacturer list.
Which regulators recognise Tenamyd Pharmaceutical's GMP?
Current GMP certificates are on record from 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