Suppliers / Vidipha Central Pharmaceutical

Vidipha Central Pharmaceutical

Vietnam Updated 9 July 2026

Vidipha Central Pharmaceutical is an API manufacturer based in Vietnam. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file.

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

What they file, and where

Molecule Regulators Docs
Enalapril DAV (Vietnam) 1

Also appears on these molecule pages

Enalapril API

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 1 None

Questions about Vidipha Central Pharmaceutical

Does Vidipha Central Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Vidipha Central Pharmaceutical. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Vidipha Central Pharmaceutical make?
1 molecule is on record against Vidipha Central Pharmaceutical, including Enalapril. Each links through to that molecule's full manufacturer list.
Where does Vidipha Central Pharmaceutical file?
Filings are on record with DAV (Vietnam), 1 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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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