Suppliers / Unicorn International

Unicorn International

Updated 9 July 2026

Unicorn International is a finished-dose manufacturer. It appears in 317 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with DH (HK) and BRELA (TZ).

0
active US DMFs
0
valid CEPs
0
registered plants
317
filings across 2 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
DH (HK) 315 None
BRELA (TZ) 2 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Unicorn International

Does Unicorn International hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Unicorn International. It does have 317 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Unicorn International file?
Filings are on record with DH (HK) and BRELA (TZ), 317 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?

Choose your molecules and target markets. Unicorn International comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability