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.
183
filings
across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
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