Suppliers / Công Ty TNHH Liên Doanh Stellapharm

Công Ty TNHH Liên Doanh Stellapharm

Vietnam Updated 9 July 2026

Công Ty TNHH Liên Doanh Stellapharm is an API and finished-dose manufacturer based in Vietnam. It appears in 357 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
357
filings across 1 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 357 None

Questions about Công Ty TNHH Liên Doanh Stellapharm

Does Công Ty TNHH Liên Doanh Stellapharm hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Công Ty TNHH Liên Doanh Stellapharm. It does have 357 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Công Ty TNHH Liên Doanh Stellapharm make?
5 molecules are on record against Công Ty TNHH Liên Doanh Stellapharm, including Lisinopril, Fluocinolone Acetonide, Glimepiride and Magnesium Hydroxide. Each links through to that molecule's full manufacturer list.
Where does Công Ty TNHH Liên Doanh Stellapharm file?
Filings are on record with DAV (Vietnam), 357 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