Suppliers / Công Ty Cổ Phần Kỹ Thuật Dược Bình Định

Công Ty Cổ Phần Kỹ Thuật Dược Bình Định

Vietnam Updated 9 July 2026

Công Ty Cổ Phần Kỹ Thuật Dược Bình Định is an API and finished-dose manufacturer based in Vietnam. It appears in 21 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
21
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Dextrose DAV (Vietnam) 4
Natri Clorid DAV (Vietnam) 4
Glutamic Acid DAV (Vietnam) 2
Natri Lactat DAV (Vietnam) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 21 None

Questions about Công Ty Cổ Phần Kỹ Thuật Dược Bình Định

Does Công Ty Cổ Phần Kỹ Thuật Dược Bình Định hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Công Ty Cổ Phần Kỹ Thuật Dược Bình Định. It does have 21 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 Kỹ Thuật Dược Bình Định make?
4 molecules are on record against Công Ty Cổ Phần Kỹ Thuật Dược Bình Định, including Dextrose, Natri Clorid, Glutamic Acid and Natri Lactat. Each links through to that molecule's full manufacturer list.
Where does Công Ty Cổ Phần Kỹ Thuật Dược Bình Định file?
Filings are on record with DAV (Vietnam), 21 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