Suppliers / Công Ty Cổ Phần Dược Enlie (Enlie Pharma)

Công Ty Cổ Phần Dược Enlie (Enlie Pharma)

Vietnam Updated 9 July 2026

Công Ty Cổ Phần Dược Enlie (Enlie Pharma) is an API and finished-dose manufacturer based in Vietnam. It appears in 83 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
83
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Trazodone DAV (Vietnam) 2
Cetirizine DAV (Vietnam) 1
Cinnarizine DAV (Vietnam) 1
Dapagliflozin DAV (Vietnam) 1
Dimenhydrinate DAV (Vietnam) 1
Entecavir DAV (Vietnam) 1
Lansoprazole DAV (Vietnam) 1
Magnesium Pidolate DAV (Vietnam) 1
Otilonium Bromide DAV (Vietnam) 1
Propranolol DAV (Vietnam) 1
Show all 17 molecules on file
Pyridoxine DAV (Vietnam) 1
Rebamipid DAV (Vietnam) 1
Rupatadine DAV (Vietnam) 1
Ticagrelor DAV (Vietnam) 1
Tofisopam DAV (Vietnam) 1
Trimethoprim DAV (Vietnam) 1
Valganciclovir 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) 83 None

Questions about Công Ty Cổ Phần Dược Enlie (Enlie Pharma)

Does Công Ty Cổ Phần Dược Enlie (Enlie Pharma) hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Công Ty Cổ Phần Dược Enlie (Enlie Pharma). It does have 83 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Công Ty Cổ Phần Dược Enlie (Enlie Pharma) make?
17 molecules are on record against Công Ty Cổ Phần Dược Enlie (Enlie Pharma), including Trazodone, Cetirizine, Cinnarizine and Dapagliflozin. Each links through to that molecule's full manufacturer list.
Where does Công Ty Cổ Phần Dược Enlie (Enlie Pharma) file?
Filings are on record with DAV (Vietnam), 83 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