Suppliers / Công ty cổ phần dược Đồng Nai (Donaipharm)

Công ty cổ phần dược Đồng Nai (Donaipharm)

Vietnam Updated 9 July 2026

Công ty cổ phần dược Đồng Nai (Donaipharm) is an API and finished-dose manufacturer based in Vietnam. It appears in 164 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
164
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Cetirizine DAV (Vietnam) 1
Domperidone DAV (Vietnam) 1
Doxycycline DAV (Vietnam) 1
Rupatadine DAV (Vietnam) 1
Tramadol DAV (Vietnam) 1

Also appears on these molecule pages

Alverine finished dose Nefopam finished dose Cetirizine API Tramadol API Doxycycline API Domperidone API Rupatadine API

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 164 None

Questions about Công ty cổ phần dược Đồng Nai (Donaipharm)

Does Công ty cổ phần dược Đồng Nai (Donaipharm) 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 Đồng Nai (Donaipharm). It does have 164 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 Đồng Nai (Donaipharm) make?
5 molecules are on record against Công ty cổ phần dược Đồng Nai (Donaipharm), including Cetirizine, Domperidone, Doxycycline and Rupatadine. Each links through to that molecule's full manufacturer list.
Where does Công ty cổ phần dược Đồng Nai (Donaipharm) file?
Filings are on record with DAV (Vietnam), 164 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.

Comparing suppliers?

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Comparable suppliers

Danapha Pharmaceutical Joint Stock also in Vietnam Fremed Pharmaceutical Joint Stock also in Vietnam Hanoi Cpc1 Pharmaceutical Joint Stock also in Vietnam Imexpharm also in Vietnam Minh also in Vietnam

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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