Suppliers / Công ty cổ phần dược phẩm Quảng Bình

Công ty cổ phần dược phẩm Quảng Bình

Vietnam Updated 9 July 2026

Công ty cổ phần dược phẩm Quảng Bình is an API and finished-dose manufacturer based in Vietnam. It appears in 219 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
219
filings across 1 regulators

What they file, and where

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 219 None

Questions about Công ty cổ phần dược phẩm Quảng Bình

Does Công ty cổ phần dược phẩm Quảng Bình 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 Quảng Bình. It does have 219 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 Quảng Bình make?
7 molecules are on record against Công ty cổ phần dược phẩm Quảng Bình, including Acetaminophen, Acyclovir, Dexamethasone and Ezetimibe. Each links through to that molecule's full manufacturer list.
Where does Công ty cổ phần dược phẩm Quảng Bình file?
Filings are on record with DAV (Vietnam), 219 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