Suppliers / Công ty Cổ phần Dược phẩm Gia Nguyễn

Công ty Cổ phần Dược phẩm Gia Nguyễn

Vietnam Updated 9 July 2026

Công ty Cổ phần Dược phẩm Gia Nguyễn is an API and finished-dose manufacturer based in Vietnam. It appears in 38 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
38
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Acyclovir DAV (Vietnam) 3
Metronidazole DAV (Vietnam) 2
Spiramycin DAV (Vietnam) 2
Terbinafine DAV (Vietnam) 2
Xylometazoline DAV (Vietnam) 2
Acetylcysteine DAV (Vietnam) 1
Azelastine DAV (Vietnam) 1
Betamethasone DAV (Vietnam) 1
Clobetasol Propionate DAV (Vietnam) 1
Febuxostat DAV (Vietnam) 1
Show all 19 molecules on file
Fexofenadine DAV (Vietnam) 1
Folic Acid DAV (Vietnam) 1
Methionine DAV (Vietnam) 1
Polymyxin B DAV (Vietnam) 1
Tacrolimus DAV (Vietnam) 1
Tetryzoline DAV (Vietnam) 1
Threonine DAV (Vietnam) 1
Triamcinolone DAV (Vietnam) 1
Vitamin E DAV (Vietnam) 1

Also appears on these molecule pages

Show 6 more molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 38 None

Questions about Công ty Cổ phần Dược phẩm Gia Nguyễn

Does Công ty Cổ phần Dược phẩm Gia Nguyễn 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 phẩm Gia Nguyễn. It does have 38 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 phẩm Gia Nguyễn make?
19 molecules are on record against Công ty Cổ phần Dược phẩm Gia Nguyễn, including Acyclovir, Metronidazole, Spiramycin and Terbinafine. Each links through to that molecule's full manufacturer list.
Where does Công ty Cổ phần Dược phẩm Gia Nguyễn file?
Filings are on record with DAV (Vietnam), 38 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