Suppliers / Công ty Cổ phần Dược phẩm công nghệ cao Abipha

Công ty Cổ phần Dược phẩm công nghệ cao Abipha

Vietnam Updated 9 July 2026

Công ty Cổ phần Dược phẩm công nghệ cao Abipha is an API and finished-dose manufacturer based in Vietnam. It appears in 89 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
89
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Metronidazole DAV (Vietnam) 2
Acetylcysteine DAV (Vietnam) 1
Piracetam DAV (Vietnam) 1
Pitavastatin DAV (Vietnam) 1
Pyridoxine DAV (Vietnam) 1

Also appears on these molecule pages

Dexibuprofen finished dose Metronidazole API Piracetam API Pitavastatin API Vinpocetine finished dose Acetylcysteine API

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 89 None

Questions about Công ty Cổ phần Dược phẩm công nghệ cao Abipha

Does Công ty Cổ phần Dược phẩm công nghệ cao Abipha 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 công nghệ cao Abipha. It does have 89 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 công nghệ cao Abipha make?
5 molecules are on record against Công ty Cổ phần Dược phẩm công nghệ cao Abipha, including Metronidazole, Acetylcysteine, Piracetam and Pitavastatin. Each links through to that molecule's full manufacturer list.
Where does Công ty Cổ phần Dược phẩm công nghệ cao Abipha file?
Filings are on record with DAV (Vietnam), 89 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

Imexpharm shares 2 molecules MSN Laboratories shares 1 molecule Apitoria Pharma shares 1 molecule Hetero shares 1 molecule Matrix Pharmacorp 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