Suppliers / Công ty cổ phần dược Hà Tĩnh

Công ty cổ phần dược Hà Tĩnh

Vietnam Updated 9 July 2026

Công ty cổ phần dược Hà Tĩnh is an API and finished-dose manufacturer based in Vietnam. It appears in 270 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
270
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Rivaroxaban DAV (Vietnam) 2
Rupatadine DAV (Vietnam) 2
Acetaminophen DAV (Vietnam) 1
Acetylcysteine DAV (Vietnam) 1
Berberine DAV (Vietnam) 1
Betamethasone DAV (Vietnam) 1
Cafein DAV (Vietnam) 1
Ciprofloxacin DAV (Vietnam) 1
Clobetasone DAV (Vietnam) 1
Codeine DAV (Vietnam) 1
Show all 22 molecules on file
Dextromethorphan DAV (Vietnam) 1
Erythromycin DAV (Vietnam) 1
Ibuprofen DAV (Vietnam) 1
Mecobalamin DAV (Vietnam) 1
Methylprednisolone DAV (Vietnam) 1
Moxifloxacin DAV (Vietnam) 1
Prednisolone DAV (Vietnam) 1
Pyridoxine DAV (Vietnam) 1
Rebamipid DAV (Vietnam) 1
Sildenafil DAV (Vietnam) 1
Tacrolimus DAV (Vietnam) 1
Terbutaline DAV (Vietnam) 1

Also appears on these molecule pages

Show 8 more molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 270 None

Questions about Công ty cổ phần dược Hà Tĩnh

Does Công ty cổ phần dược Hà Tĩnh 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 Hà Tĩnh. It does have 270 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 Hà Tĩnh make?
22 molecules are on record against Công ty cổ phần dược Hà Tĩnh, including Rivaroxaban, Rupatadine, Acetaminophen and Acetylcysteine. Each links through to that molecule's full manufacturer list.
Where does Công ty cổ phần dược Hà Tĩnh file?
Filings are on record with DAV (Vietnam), 270 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