Suppliers / Công ty Cổ phần Dược phẩm Meracine

Công ty Cổ phần Dược phẩm Meracine

Vietnam 79 employees Updated 9 July 2026

Công ty Cổ phần Dược phẩm Meracine is an API manufacturer based in Vietnam. It appears in 64 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
64
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Acetaminophen DAV (Vietnam) 2
Celecoxib DAV (Vietnam) 1
Duloxetine DAV (Vietnam) 1
Gentamicin DAV (Vietnam) 1
Lipoic Acid DAV (Vietnam) 1
Sildenafil DAV (Vietnam) 1
Tobramycin DAV (Vietnam) 1
Xylometazoline DAV (Vietnam) 1

Also appears on these molecule pages

Gentamicin API Lipoic Acid API Tobramycin API Xylometazoline API Paracetamol API Celecoxib API Sildenafil API Duloxetine API

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 64 None

Questions about Công ty Cổ phần Dược phẩm Meracine

Does Công ty Cổ phần Dược phẩm Meracine 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 Meracine. It does have 64 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 Meracine make?
8 molecules are on record against Công ty Cổ phần Dược phẩm Meracine, including Acetaminophen, Celecoxib, Duloxetine and Gentamicin. Each links through to that molecule's full manufacturer list.
Where does Công ty Cổ phần Dược phẩm Meracine file?
Filings are on record with DAV (Vietnam), 64 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

Livzon Group Fuzhou Fuxing Pharmaceutical shares 2 molecules Olon shares 1 molecule Acs Dobfar shares 1 molecule Siegfried shares 1 molecule Ami Lifesciences shares 1 molecule

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